Tag intelligence

Dermatology reimbursement alerts

Reimbursement alerts filtered by specialty and region tags for faster analysis across coding, compliance, and revenue integrity.

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Overview

50 alerts match the tag Dermatology. Review high-value policy alerts and the underlying claims guidance that matters.

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Alert count

50

Distinct policy codes

50

Average signal score

61

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50 shown · 50 total in platform

Risk: Elevated
0

Critical

0%

33

High

66%

17

Routine

34%

0

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LCD L33563: Incision and Drainage (I & D) of Abscess of Skin, Subcutaneous and Accessory Structures — Wellpoint Federal

Policy LCD-L33563Dermatology

High

This active final LCD from Wellpoint Federal governs coverage criteria for Incision and Drainage (I&D) of abscesses involving skin, subcutaneous tissue, and accessory structures, effective April 1, 20

FDA Approval: DUPIXENT (DUPILUMAB) — Type 1 - New Molecular Entity

Policy FDA-BLA761055Dermatology

High

Dupixent (dupilumab) is an injectable interleukin-4 receptor alpha antagonist approved for subcutaneous administration, placing it on the Part B billing pathway for physician-administered claims. Bill

FDA Approval: ILUMYA (TILDRAKIZUMAB-ASMN) — Type 1 - New Molecular Entity

Policy FDA-BLA761067Dermatology

High

Ilumya (tildrakizumab-asmn) is an injectable interleukin-23 antagonist approved for plaque psoriasis, administered via subcutaneous injection in a physician office or clinical setting, supporting Part

FDA Approval: USTEKINUMAB (USTEKINUMAB) — Type 1 - New Molecular Entity

Policy FDA-BLA125261Dermatology

High

Ustekinumab (Stelara) is an injectable interleukin-12/23 antagonist approved via BLA125261, administered by injection and billed under Medicare Part B. As an injectable biologic administered in a phys

FDA Approval: ELOCON (MOMETASONE FUROATE) — Type 3 - New Dosage Form

Policy FDA-NDA019625Dermatology

Routine

Elocon (mometasone furoate) is a topical corticosteroid cream approved under NDA019625, billing through Medicare Part D as a self-administered topical medication. As a long-established brand with exte

FDA Approval: ELOCON (MOMETASONE FUROATE) — Type 3 - New Dosage Form

Policy FDA-NDA019796Dermatology

Routine

Elocon (mometasone furoate) Lotion is a topical corticosteroid approved under NDA019796, administered via the topical route, placing it squarely in the Part D billing pathway as a self-administered ou

FDA Approval: ELOCON (MOMETASONE FUROATE) — Type 1 - New Molecular Entity

Policy FDA-NDA019543Dermatology

Routine

Elocon (mometasone furoate) is a topical corticosteroid ointment approved in 1987, administered topically and billed under Medicare Part D as a self-administered drug. As a long-established branded to

FDA Approval: ZORYVE (ROFLUMILAST) — Type 3 - New Dosage Form

Policy FDA-NDA215985Dermatology

Routine

ZORYVE (roflumilast) 0.3% cream was approved by the FDA on July 29, 2022, as a topical phosphodiesterase 4 inhibitor indicated for plaque psoriasis. As a topical cream, this product follows the Part D

FDA Approval: ANZUPGO (DELGOCITINIB) — Type 1 - New Molecular Entity

Policy FDA-NDA219155Dermatology

Routine

Anzupgo (delgocitinib) is a topical JAK inhibitor cream approved as a new molecular entity, with a clear Part D billing pathway as a self-administered topical drug. It will be dispensed through retail

FDA Approval: CIBINQO (ABROCITINIB) — Type 1 - New Molecular Entity

Policy FDA-NDA213871Dermatology

Routine

Cibinqo (abrocitinib), an oral Janus Kinase Inhibitor approved for atopic dermatitis, follows a Part D billing pathway as an oral tablet dispensed through retail or specialty pharmacy. Because this is

FDA Approval: LITFULO (RITLECITINIB) — Type 1 - New Molecular Entity

Policy FDA-NDA215830Dermatology

Routine

Litfulo (ritlecitinib) is an oral capsule approved via NDA215830 and follows a Part D billing pathway, meaning it is dispensed through retail or specialty pharmacies rather than administered in a clin

FDA Approval: SOTYKTU (DEUCRAVACITINIB) — Type 1 - New Molecular Entity

Policy FDA-NDA214958Dermatology

Routine

Sotyktu (deucravacitinib) is an oral tablet approved as a new molecular entity, placing it squarely in the Medicare Part D billing pathway as a self-administered drug. As a branded oral specialty medi

FDA Approval: LEQSELVI (DEURUXOLITINIB PHOSPHATE) — Type 1 - New Molecular Entity

Policy FDA-NDA217900Dermatology

Routine

Leqselvi (deuruxolitinib phosphate) was approved by the FDA on July 25, 2024, as an oral tablet, placing it squarely in the Medicare Part D billing pathway as a self-administered drug. As a new molecu

FDA Approval: OPZELURA (RUXOLITINIB) — Type 10 - New Indication Submitted as Distinct NDA - Not Consolidated

Policy FDA-NDA215309Dermatology

Routine

Opzelura (ruxolitinib) cream received FDA approval via NDA215309 as a topical formulation, placing it firmly in the Medicare Part D billing pathway as a self-administered drug. As a topical cream, it

FDA Approval: SKYRIZI (RISANKIZUMAB-RZAA) — Type 3 - New Dosage Form

Policy FDA-BLA761262Dermatology

High

SKYRIZI (risankizumab-rzaa) is an injectable drug approved for use under Medicare Part B, likely leading to the assignment of a new J-code for billing purposes. As an orphan drug in the interleukin-23

FDA Approval: SKYRIZI (RISANKIZUMAB-RZAA) — Type 1 - New Molecular Entity

Policy FDA-BLA761105Dermatology

High

SKYRIZI (Risankizumab-rzaa), being an injectable drug approved under the BLA, is likely to be assigned a J-code for Medicare billing. Given its classification as an orphan drug and its high cost, pass

FDA Approval: ZYRTEC HIVES (CETIRIZINE HYDROCHLORIDE) — Type 1 - New Molecular Entity

Policy FDA-NDA019835Dermatology

Routine

CETIRIZINE HYDROCHLORIDE, marketed as ZYRTEC HIVES, is an oral drug and will be billed under Medicare Part D. Given that it is not an injectable drug, no J-code will be assigned, and typical reimburse

FDA Approval: ABSORICA (ISOTRETINOIN) — Type 3 - New Dosage Form

Policy FDA-NDA021951Dermatology

Routine

As ABSORICA (isotretinoin) is an oral drug, it will be billed under Medicare Part D. Given that it is a medication used for severe acne, prescribers should consider any prior authorizations or step th

FDA Approval: EBGLYSS (LEBRIKIZUMAB-LBKZ) — Type 1 - New Molecular Entity

Policy FDA-BLA761306Dermatology

High

EBGLYSS (LBRIKIZUMAB-LBKZ) will be billed under Part B as it is an injectable drug. Billing teams should confirm the specifics of the J-code upon the release of the FDA label.

Proposed LCD DL40176: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — Noridian

Policy LCD-DL40176Dermatology

Routine

The proposed Local Coverage Determination (LCD) for Superficial Radiation Therapy (SRT) will impact billing by potentially increasing reimbursement for treatments of nonmelanoma skin cancers. It aims

Proposed LCD DL40189: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — Palmetto GBA

Policy LCD-DL40189Dermatology

Routine

The proposed Local Coverage Determination (LCD) for Superficial Radiation Therapy (SRT) could significantly influence reimbursement levels for procedures related to Nonmelanoma Skin Cancers. Providers

Proposed LCD DL40168: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — NGS

Policy LCD-DL40168Dermatology

Routine

The proposed LCD for Superficial Radiation Therapy (SRT) for Nonmelanoma Skin Cancers will likely expand coverage options, promoting more access to this treatment modality. This could positively impac

Proposed LCD DL40179: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — CGS

Policy LCD-DL40179Dermatology

Routine

The proposed LCD for Superficial Radiation Therapy (SRT) may impact billing by clarifying coverage terms for treatment of Nonmelanoma Skin Cancers (NMSC). This requires billing team review

Proposed LCD DL40193: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — WPS

Policy LCD-DL40193Dermatology

Routine

The proposed LCD for Superficial Radiation Therapy (SRT) will likely supports compliance with updated rates options for providers treating Nonmelanoma Skin Cancers (NMSC). This inclusion may lead to increased utilizat

LCD L37725: MolDX: Melanoma Risk Stratification Molecular Testing — Palmetto GBA

Policy LCD-L37725Dermatology

High

The upcoming LCD for Melanoma Risk Stratification may significantly impact billing practices for providers conducting molecular testing. It sets clear guidelines for coverage, ensuring appropriate rei

LCD L38016: MolDX: Melanoma Risk Stratification Molecular Testing — CGS

Policy LCD-L38016Dermatology

High

The introduction of the MolDX Melanoma Risk Stratification Molecular Testing is expected to enhance precision in melanoma diagnostics, potentially leading to more tailored treatment plans. Providers s

LCD L34200: Removal of Benign Skin Lesions — CGS

Policy LCD-L34200Dermatology

High

The new Local Coverage Determination (LCD) for the removal of benign skin lesions by CGS may impact billing practices in dermatology, leading to increased scrutiny on claims for these procedures. Prov

LCD L38904: Wound and Ulcer Care — Noridian

Policy LCD-L38904Dermatology

High

The recent LCD on Wound and Ulcer Care may lead to supports compliance with updated rates processes, particularly for claims related to wound management. Proper documentation and adherence to the outlined

LCD L35163: Plastic Surgery — Noridian

Policy LCD-L35163Dermatology

High

The introduction of the new LCD for Plastic Surgery by Noridian effective October 16, 2025, may significantly impact billing processes, affecting reimbursement rates and procedures allowable under Med

LCD L35702: Mohs Micrographic Surgery — Noridian

Policy LCD-L35702Dermatology

High

The introduction of Mohs Micrographic Surgery (MMS) by Noridian will enhance compliance updates for dermatology practices. This update is expected to improve reimbursement rates and streamline the

LCD L34233: Benign Skin Lesion Removal (Excludes Actinic Keratosis, and Mohs) — Noridian

Policy LCD-L34233Dermatology

High

The new LCD for benign skin lesion removal may alter billing practices, particularly for cases excluding actinic keratosis and Mohs surgery. Providers should be aware of potential changes in reimburse

LCD L37020: Plastic Surgery — Noridian

Policy LCD-L37020Dermatology

High

The new LCD from Noridian introduces updated guidelines for plastic surgery billing, which may affect reimbursement rates and claims processing. Providers should review the changes to ensure complianc

LCD L33445: Removal of Benign and Malignant Skin Lesions — Palmetto GBA

Policy LCD-L33445Dermatology

High

The implementation of the LCD for the removal of benign and malignant skin lesions by Palmetto GBA may affect billing practices starting from October 23, 2025. Providers will need to ensure compliance

LCD L35498: Removal of Benign Skin Lesions — WPS

Policy LCD-L35498Dermatology

High

The upcoming Local Coverage Determination (LCD) on the removal of benign skin lesions will clarify billing guidelines, potentially impacting reimbursement patterns for dermatology services. Providers

LCD L35704: Mohs Micrographic Surgery — Noridian

Policy LCD-L35704Dermatology

High

The Noridian LCD for Mohs Micrographic Surgery outlines specific billing requirements that could affect reimbursements if not followed accurately. Adhering to these guidelines is crucial for ensuring

LCD L33979: Benign Skin Lesion Removal (Excludes Actinic Keratosis, and Mohs) — Noridian

Policy LCD-L33979Dermatology

High

The LCD for benign skin lesion removal may lead to an increase in denied claims if providers do not adhere strictly to the guidelines excluding actinic keratosis and Mohs procedures. Ensuring proper d

LCD L39589: MolDX: Molecular Biomarker Testing for Risk Stratification of Cutaneous Squamous Cell Carcinoma — Noridian

Policy LCD-L39589Dermatology

High

The new LCD from Noridian outlines guidelines for MolDX testing in cutaneous squamous cell carcinoma, which could impact reimbursement practices for genetic testing procedures. Billing for these servi

LCD L39373: MolDX: Molecular Assays for the Diagnosis of Cutaneous Melanoma — Noridian

Policy LCD-L39373Dermatology

High

The introduction of the MolDX for the diagnosis of cutaneous melanoma may significantly impact billing practices for pathology services in dermatology. Providers may need to adapt to new HCPCS and ICD

LCD L39594: MolDX: Molecular Biomarker Testing for Risk Stratification of Cutaneous Squamous Cell Carcinoma — Noridian

Policy LCD-L39594Dermatology

High

The implementation of the new LCD for molecular biomarker testing in cutaneous squamous cell carcinoma may lead to supports compliance with updated rates, potentially impacting overall billin

LCD L38151: MolDX: Pigmented Lesion Assay — Noridian

Policy LCD-L38151Dermatology

High

The implementation of the MolDX: Pigmented Lesion Assay may significantly impact billing practices, as it introduces specific coding requirements that must be adhered to in order to ensure appropriate

LCD L38153: MolDX: Pigmented Lesion Assay — Noridian

Policy LCD-L38153Dermatology

High

The implementation of the MolDX: Pigmented Lesion Assay effective June 20, 2024, may introduce new billing procedures for providers. This could lead to changes in reimbursement patterns and necessitat

LCD L40176: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — Noridian

Policy LCD-L40176Dermatology

High

The new Local Coverage Determination (LCD) for Superficial Radiation Therapy (SRT) will provide clearer guidelines for billing related to Nonmelanoma Skin Cancers (NMSC). Effective from March 1, 2026,

LCD L40189: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — Palmetto GBA

Policy LCD-L40189Dermatology

High

The new local coverage determination (LCD) for Superficial Radiation Therapy could impact reimbursement for treatments of nonmelanoma skin cancers starting March 1, 2026. Facilities should prepare for

LCD L40168: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — NGS

Policy LCD-L40168Dermatology

High

The implementation of Superficial Radiation Therapy (SRT) for Nonmelanoma Skin Cancers (NMSC) requires billing team review. Effective from March 1, 202

LCD L40193: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — WPS

Policy LCD-L40193Dermatology

High

The introduction of the LCD for Superficial Radiation Therapy (SRT) will positively influence billing by ensuring clear guidelines for reimbursement related to Nonmelanoma Skin Cancers (NMSC). Provide

LCD L40179: Superficial Radiation Therapy (SRT) for the Treatment of Nonmelanoma Skin Cancers (NMSC) — CGS

Policy LCD-L40179Dermatology

High

The new LCD on Superficial Radiation Therapy for Nonmelanoma Skin Cancers may lead to increased compliance updates for providers offering this treatment. However, it is essential to ensure proper d

LCD L38178: MolDX: Pigmented Lesion Assay — WPS

Policy LCD-L38178Dermatology

High

The MolDX Pigmented Lesion Assay will have a significant impact on billing practices starting April 30, 2026. Providers must ensure they are familiar with the associated HCPCS and ICD-10 codes to opti

LCD L34195: Mohs Micrographic Surgery — CGS

Policy LCD-L34195Dermatology

High

The final LCD L34195 relates to Mohs Micrographic Surgery and is now active. Providers in Kentucky and Ohio should ensure compliance with this policy effective May 7, 2026, regarding billing under Par

LCD L39506: Cosmetic and Reconstructive Surgery — CGS Administrators

Policy LCD-L39506Dermatology

High

This LCD covers guidelines for billing cosmetic and reconstructive surgery services under Medicare. It affects both Part A and Part B claims, indicating specific criteria that must be met for procedur

FDA Approval: TREMFYA (GUSELKUMAB) — Type 1 - New Molecular Entity

Policy FDA-BLA761061Dermatology

High

Tremfya (Guselkumab) is an injectable drug that will likely be assigned a J-code for Medicare billing. As a Part B candidate, it may also be subject to ASP+6% reimbursement rates. Providers should be