PUBLIX Regular Strength

UNIISPL

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

Identification

ManufacturerPUBLIX SUPER MARKETS, INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
4141570608
236 mL in 1 BOTTLE (41415-706-08)
ndc11
4141570616
473 mL in 1 BOTTLE (41415-706-16)

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": {
    "f5d1394b-0fe8-c372-e053-2a95a90a1f78": {
      "match": "brand_token",
      "title": "PUBLIX ARTIFICIAL TEARS EYE DROPS (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [PUBLIX SUPER MARKETS, INC.]",
      "spl_version": "3",
      "published_date": "2026-01-02"
    }
  },
  "productid": "41415-706_42375585-2843-fa23-e063-6294a90af057",
  "productndc": "41415-706",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH SUBSALICYLATE",
  "proprietary_name": "PUBLIX Regular Strength",
  "active_ingred_unit": "mg/30mL",
  "application_number": "M008",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Bismuth Subsalicylate",
  "start_marketing_date": "20221024",
  "active_numerator_strength": "525"
}

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