Walgreens Advanced Scar Gel

UNIISPL

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

Identification

ManufacturerWalgreens Company

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0363231207
1 TUBE in 1 CARTON (0363-2312-07) / 20 g in 1 TUBE

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": "TOPICAL",
  "spl_meta": {
    "34952272-1f9e-c642-e063-6394a90ae2bd": {
      "match": "brand_token",
      "title": "WALGREENS SCALP ITCH RELIEF (HYDROCORTISONE) LIQUID [WALGREENS]",
      "spl_version": "2",
      "published_date": "2026-06-01"
    }
  },
  "productid": "0363-2312_fbca3a59-215c-4b21-845e-e175e345cf3a",
  "productndc": "0363-2312",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "Walgreens Advanced Scar Gel",
  "active_ingred_unit": "mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Advanced Scar Gel",
  "start_marketing_date": "20190326",
  "active_numerator_strength": "5"
}

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