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United States · US · US:70677-1242_498af382-ead9-9b5d-e063-6294a90a7852
EXTRA STRENGTH PAIN RELEIF
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerStrategic Sourcing Services, LLC
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117067712421120 TABLET, FILM COATED in 1 BOTTLE (70677-1242-1)
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": "70677-1242_498af382-ead9-9b5d-e063-6294a90a7852",
"productndc": "70677-1242",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "EXTRA STRENGTH PAIN RELEIF",
"active_ingred_unit": "mg/1",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "ACETAMINOPHEN",
"start_marketing_date": "20240202",
"active_numerator_strength": "500"
}Related drugs
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