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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
- ndc111182270702354 mL in 1 BOTTLE (11822-7070-2)
- ndc111182270708236 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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