Digestive Relief

UNIISPL

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

Identification

ManufacturerSAFEWAY

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
2113012540
1 BOTTLE in 1 CARTON (21130-125-40) / 40 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)

62TEY51RR1

BISMUTH SUBSALICYLATE

RxCUI 19478

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "62TEY51RR1",
    "rxcui": "19478",
    "inchikey": "ZREIPSZUJIFJNP-UHFFFAOYSA-K",
    "display_name": "BISMUTH SUBSALICYLATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "74ce6879-ca7f-4664-949b-94abca92bc67": {
      "match": "brand_token",
      "title": "DIGESTIVE ENZYME LIQUESCENCE 3007 (DIGESTIVE ENZYME LIQUESCENCE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "21130-125_424aa911-6748-010b-e063-6394a90a7ae7",
  "productndc": "21130-125",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH SUBSALICYLATE",
  "proprietary_name": "Digestive Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "M008",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Bismuth Subsalicylate",
  "start_marketing_date": "20201005",
  "active_numerator_strength": "262"
}

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