Walgreens Fast Acting Heartburn Relief Extra Strength

UNIISPL

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

Identification

ManufacturerWALGREEN CO.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0363763012
355 mL in 1 BOTTLE (0363-7630-12)

Annotations

UNII (FDA Substance ID)

5QB0T2IUN0

ALUMINUM HYDROXIDE

RxCUI 81948

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "5QB0T2IUN0",
    "rxcui": "81948",
    "inchikey": "WNROFYMDJYEPJX-UHFFFAOYSA-K",
    "display_name": "ALUMINUM HYDROXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "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": "0363-7630_447ce367-bceb-756d-e063-6294a90a4bb7",
  "productndc": "0363-7630",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE",
  "proprietary_name": "Walgreens Fast Acting Heartburn Relief Extra Strength",
  "active_ingred_unit": "mg/5mL; mg/5mL",
  "application_number": "M001",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "aluminum hydroxide and magnesium carbonate",
  "start_marketing_date": "20180115",
  "active_numerator_strength": "254; 237.5"
}

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