Ultra Stomach Relief

UNIISPL

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

Identification

ManufacturerSafeway, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
2113066208
237 mL in 1 BOTTLE, PLASTIC (21130-662-08)
ndc11
2113066212
355 mL in 1 BOTTLE, PLASTIC (21130-662-12)

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": "21130-662_fc7c84ee-b7a2-47bb-9227-15e4ea248653",
  "productndc": "21130-662",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH SUBSALICYLATE",
  "proprietary_name": "Ultra Stomach Relief",
  "active_ingred_unit": "mg/15mL",
  "application_number": "M008",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Bismuth subsalicylate",
  "start_marketing_date": "20191129",
  "active_numerator_strength": "525"
}

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