Pepto Bismol

UNIISPL

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

Identification

ManufacturerThe Procter & Gamble Manufacturing Company

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
3700053712
1 BLISTER PACK in 1 CARTON (37000-537-12) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
ndc11
3700053748
4 BLISTER PACK in 1 CARTON (37000-537-48) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

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": {
    "84ffa6d6-03e1-59e8-e053-2a91aa0afd6e": {
      "match": "brand_token",
      "title": "PEPTO BISMOL LIQUICAPS (BISMUTH SUBSALICYLATE) CAPSULE, LIQUID FILLED [THE PROCTER & GAMBLE MANUFACTURING COMPANY]",
      "spl_version": "12",
      "published_date": "2026-04-27"
    }
  },
  "productid": "37000-537_0b3cb53e-1d79-f343-e063-6394a90a17ca",
  "productndc": "37000-537",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH SUBSALICYLATE",
  "proprietary_name": "Pepto Bismol",
  "active_ingred_unit": "mg/1",
  "application_number": "M008",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Bismuth subsalicylate",
  "start_marketing_date": "20180301",
  "active_numerator_strength": "262"
}

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