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United States · US · US:0135-0539_10c14ee5-017b-0434-e063-6394a90af0f4
PANADOL
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHaleon US Holdings LLC
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1101350539021 BOTTLE in 1 CARTON (0135-0539-02) / 54.7 mL in 1 BOTTLE
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": {
"341761b9-f0be-f816-e063-6394a90a5e63": {
"match": "brand_token",
"title": "PANADOL COLD AND FLU DAY (ACETAMINOPHEN, DEXTROMETHORPHAN HBR) TABLET [HALEON US HOLDINGS LLC]",
"spl_version": "2",
"published_date": "2026-04-30"
}
},
"productid": "0135-0539_10c14ee5-017b-0434-e063-6394a90af0f4",
"productndc": "0135-0539",
"dosage_form": "SUSPENSION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "PANADOL",
"active_ingred_unit": "mg/5mL",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "acetaminophen",
"start_marketing_date": "20121015",
"active_numerator_strength": "160"
}Related drugs
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