5-Symptom Digestive Relief

UNIISPL

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

Identification

ManufacturerTARGET CORPORATION

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
1167329106
236 mL in 1 BOTTLE, PLASTIC (11673-291-06)
ndc11
1167329107
473 mL in 1 BOTTLE, PLASTIC (11673-291-07)
ndc11
1167329108
2 BOTTLE, PLASTIC in 1 PACKAGE (11673-291-08) / 473 mL in 1 BOTTLE, PLASTIC (11673-291-07)

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": {
    "28fba615-48ca-8d96-e063-6394a90a2797": {
      "match": "brand_token",
      "title": "5-SYMPTOM DIGESTIVE RELIEF (BISMUTH SUBSALICYLATE) SUSPENSION [TARGET CORPORATION]",
      "spl_version": "2",
      "published_date": "2025-06-16"
    }
  },
  "productid": "11673-291_32932e3f-edb6-5d92-e063-6394a90a4c43",
  "productndc": "11673-291",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH SUBSALICYLATE",
  "proprietary_name": "5-Symptom Digestive Relief",
  "active_ingred_unit": "mg/30mL",
  "application_number": "M008",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Bismuth Subsalicylate",
  "start_marketing_date": "20250616",
  "active_numerator_strength": "525"
}

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