Walgreens Acne Control Gel

UNIISPLATC S01BC08

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

Identification

ManufacturerWALGREEN COMPANY

CountryUS (United States)

ATC codeS01BC08

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0363026983
1 TUBE in 1 CARTON (0363-0269-83) / 40 mL in 1 TUBE

Annotations

UNII (FDA Substance ID)

O414PZ4LPZ

SALICYLIC ACID

RxCUI 9525

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "O414PZ4LPZ",
    "rxcui": "9525",
    "inchikey": "YGSDEFSMJLZEOE-UHFFFAOYSA-N",
    "display_name": "SALICYLIC ACID",
    "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": "0363-0269_24729761-e0eb-0a70-e063-6394a90affcf",
  "productndc": "0363-0269",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SALICYLIC ACID",
  "proprietary_name": "Walgreens Acne Control Gel",
  "active_ingred_unit": "mg/mL",
  "application_number": "M006",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "SALICYLIC ACID",
  "start_marketing_date": "20230502",
  "active_numerator_strength": "20"
}

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