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United States · US · US:66715-5680_2a838f53-0e3d-3892-e063-6394a90a23d6
Extra Strength Pain Reliever
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLil' Drug Store Products, Inc.
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1166715568041 BOTTLE, PLASTIC in 1 CARTON (66715-5680-4) / 50 TABLET, FILM COATED 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": {
"525467fb-510d-0b4b-e063-6294a90acd36": {
"match": "brand_token",
"title": "EXTRA STRENGTH TYLENOL COLD PLUS FLU MULTI-SYMPTOM NIGHTTIME (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE) LIQUID [KENVUE BRANDS LLC]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "66715-5680_2a838f53-0e3d-3892-e063-6394a90a23d6",
"productndc": "66715-5680",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "Extra Strength Pain Reliever",
"active_ingred_unit": "mg/1",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Acetaminophen 500 mg, film-coated caplet",
"start_marketing_date": "20220509",
"active_numerator_strength": "500"
}Related drugs
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