🇺🇸
United States · US · US:68788-8786_5ef18daa-ac7f-42af-9cbb-fec8469f2161
Extra Strength Pain Relief
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPreferred Pharmaceuticals Inc.
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc116878887861100 TABLET in 1 BOTTLE (68788-8786-1)
- ndc11687888786220 TABLET in 1 BOTTLE (68788-8786-2)
- ndc11687888786330 TABLET in 1 BOTTLE (68788-8786-3)
- ndc11687888786550 TABLET in 1 BOTTLE (68788-8786-5)
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": "68788-8786_5ef18daa-ac7f-42af-9cbb-fec8469f2161",
"productndc": "68788-8786",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "Extra Strength Pain Relief",
"active_ingred_unit": "mg/1",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Acetaminophen",
"start_marketing_date": "20241212",
"active_numerator_strength": "500"
}Related drugs
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