aluroderm scar

Generic: allantoin

Labeler: asclemed usa, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name aluroderm scar
Generic Name allantoin
Labeler asclemed usa, inc.
Dosage Form PATCH
Routes
CUTANEOUS
Active Ingredients

allantoin .0075 g/g

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-955
Product ID 76420-955_31b18752-52bd-1354-e063-6394a90a31f1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M016
Listing Expiration 2026-12-31
Marketing Start 2025-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420955
Hyphenated Format 76420-955

Supplemental Identifiers

RxCUI
2711688
UNII
344S277G0Z

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name aluroderm scar (source: ndc)
Generic Name allantoin (source: ndc)
Application Number M016 (source: ndc)
Routes
CUTANEOUS
source: ndc

Resolved Composition

Strengths
  • .0075 g/g
source: ndc
Packaging
  • 1 POUCH in 1 BOX (76420-955-01) / 5 PATCH in 1 POUCH / 8.5 g in 1 PATCH
source: ndc

Packages (1)

76420-955-01 1 POUCH in 1 BOX (76420-955-01) / 5 PATCH in 1 POUCH / 8.5 g in 1 PATCH

Ingredients (1)

allantoin (.0075 g/g)

Linked Drug Pages (1)

Aluroderm Scar ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["CUTANEOUS"], "spl_id": "31b18752-52bd-1354-e063-6394a90a31f1", "openfda": {"unii": ["344S277G0Z"], "rxcui": ["2711688"], "spl_set_id": ["60656ca1-5218-4595-854e-19f1061def1e"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 BOX (76420-955-01)  / 5 PATCH in 1 POUCH / 8.5 g in 1 PATCH", "package_ndc": "76420-955-01", "marketing_start_date": "20250401"}], "brand_name": "Aluroderm Scar", "product_id": "76420-955_31b18752-52bd-1354-e063-6394a90a31f1", "dosage_form": "PATCH", "product_ndc": "76420-955", "generic_name": "allantoin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aluroderm Scar", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".0075 g/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}