Aluroderm Scar

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAsclemed USA, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7642095501
1 POUCH in 1 BOX (76420-955-01) / 5 PATCH in 1 POUCH / 8.5 g in 1 PATCH

Annotations

UNII (FDA Substance ID)

344S277G0Z

ALLANTOIN

RxCUI 508

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS",
  "spl_meta": {
    "60656ca1-5218-4595-854e-19f1061def1e": {
      "match": "brand_token",
      "title": "ALURODERM SCAR (ALLANTOIN) PATCH [ASCLEMED USA, INC.]",
      "spl_version": "1",
      "published_date": "2025-04-03"
    }
  },
  "productid": "76420-955_31b18752-52bd-1354-e063-6394a90a31f1",
  "productndc": "76420-955",
  "dosage_form": "PATCH",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "Aluroderm Scar",
  "active_ingred_unit": "g/g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "allantoin",
  "start_marketing_date": "20250401",
  "active_numerator_strength": ".0075"
}

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