Ultra Strength digestive relief

UNIISPL

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

Identification

ManufacturerTHE KROGER CO.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
3014213824
1 BOTTLE in 1 CARTON (30142-138-24) / 24 TABLET 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": {
    "52d4b1c1-7431-4f8c-e063-6294a90ad482": {
      "match": "brand_token",
      "title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
      "spl_version": "1",
      "published_date": "2026-05-29"
    }
  },
  "productid": "30142-138_3b873634-dbad-e0bc-e063-6294a90a5f74",
  "productndc": "30142-138",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH SUBSALICYLATE",
  "proprietary_name": "Ultra Strength digestive relief",
  "active_ingred_unit": "mg/1",
  "application_number": "M008",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Bismuth subsalicylate",
  "start_marketing_date": "20191118",
  "active_numerator_strength": "525"
}

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