HEB Extra Strength

UNIISPL

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

Identification

ManufacturerHEB

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
3780851010
100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (37808-510-10)

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": {
    "b76c3591-6383-4661-b3db-7a56b11202f7": {
      "match": "brand_token",
      "title": "HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB]",
      "spl_version": "15",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37808-510_403e8533-17f3-670d-e063-6394a90a5b2a",
  "productndc": "37808-510",
  "dosage_form": "TABLET, CHEWABLE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE",
  "proprietary_name": "HEB Extra Strength",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "M001",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "aluminum hydroxide and magnesium carbonate",
  "start_marketing_date": "20190320",
  "active_numerator_strength": "160; 105"
}

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