HEARTBURN RELIEF

UNIISPL

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

Identification

ManufacturerCHAIN DRUG MARKETING ASSOCIATION

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6386856512
355 mL in 1 BOTTLE (63868-565-12)

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": {
    "35e12e83-5808-4f78-bcd5-33217a0d291b": {
      "match": "brand_token",
      "title": "HEARTBURN (GARLIC, BERBERIS VULGARIS ROOT, CALENDULA OFFICINALIS FLOWERING TOP, IRIS VERSICOLOR ROOT, GINGER, AND VALERIAN) SOLUTION/ DROPS [FORCES OF NATURE]",
      "spl_version": "4",
      "published_date": "2026-05-07"
    }
  },
  "productid": "63868-565_097f7264-6848-61fb-e063-6294a90a3f2f",
  "productndc": "63868-565",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE",
  "proprietary_name": "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": "20191101",
  "active_numerator_strength": "254; 237.5"
}

Access this data programmatically

Query HEARTBURN RELIEF and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs