EXTRA STRENGTH HEARTBURN RELIEF

UNIISPL

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

Identification

ManufacturerCARDINAL HEALTH

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7000003631
355 mL in 1 BOTTLE (70000-0363-1)

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": {
    "525467fb-510d-0b4b-e063-6294a90acd36": {
      "match": "brand_token",
      "title": "EXTRA STRENGTH TYLENOL COLD PLUS FLU MULTI-SYMPTOM NIGHTTIME (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE) LIQUID [KENVUE BRANDS LLC]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "70000-0363_0993a2d5-6d02-678d-e063-6394a90a2ac5",
  "productndc": "70000-0363",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE",
  "proprietary_name": "EXTRA STRENGTH HEARTBURN RELIEF",
  "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": "20190101",
  "active_numerator_strength": "254; 237.5"
}

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