🇺🇸
United States · US · US:49580-0685_f446b9fa-069b-48e1-8ae4-ec5ad945f67c
Dye Free Pain Reliever
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerP & L Development, LLC
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1149580068541 BOTTLE, PLASTIC in 1 BOX (49580-0685-4) / 118 mL in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "362O9ITL9D",
"rxcui": "161",
"inchikey": "RZVAJINKPMORJF-UHFFFAOYSA-N",
"display_name": "ACETAMINOPHEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"46846abe-062d-a11f-e063-6294a90a73f3": {
"match": "brand_token",
"title": "DYE FREE REGULAR STRENGTH STOMACH RELIEF (BISMUTH SUBSALICYLATE) SUSPENSION [WALMART INC.]",
"spl_version": "2",
"published_date": "2026-02-26"
}
},
"productid": "49580-0685_f446b9fa-069b-48e1-8ae4-ec5ad945f67c",
"productndc": "49580-0685",
"dosage_form": "SUSPENSION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "Dye Free Pain Reliever",
"active_ingred_unit": "mg/5mL",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Acetaminophen",
"start_marketing_date": "20180228",
"active_numerator_strength": "160"
}Related drugs
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