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United States · US · US:11822-7070_efd117ef-c772-40f4-aa36-e133912fada8

RITE AID Ultra Strnght

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerRITE AID CORPORATION
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    1182270702
    354 mL in 1 BOTTLE (11822-7070-2)
  • ndc11
    1182270708
    236 mL in 1 BOTTLE (11822-7070-8)

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": {
    "e285df43-317c-d862-e053-2a95a90acdce": {
      "match": "brand_token",
      "title": "RITE AID ITCH RELIEF (DIPHENHYDRAMINE HCL 2%, ZINC ACETATE 0.1%) SPRAY [RITE AID]",
      "spl_version": "4",
      "published_date": "2026-04-27"
    }
  },
  "productid": "11822-7070_efd117ef-c772-40f4-aa36-e133912fada8",
  "productndc": "11822-7070",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH SUBSALICYLATE",
  "proprietary_name": "RITE AID Ultra Strnght",
  "active_ingred_unit": "mg/15mL",
  "application_number": "M008",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Bismuth subsalicylate",
  "start_marketing_date": "20230102",
  "active_numerator_strength": "525"
}

Access this data programmatically

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