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United States · US · US:82501-0604_97b525ac-bdf4-453d-91a3-eeb7f5a1f069
GOODNOW PAIN RELIEF
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGobrands, Inc
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1182501060411 BOTTLE in 1 CARTON (82501-0604-1) / 100 TABLET, FILM COATED in 1 BOTTLE (82501-0604-0)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A072096
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WK2XYI10QM",
"rxcui": "5640",
"inchikey": "HEFNNWSXXWATRW-UHFFFAOYSA-N",
"display_name": "IBUPROFEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"7e719c06-7cf9-4d0d-84b0-d1c375ed9c76": {
"match": "brand_token",
"title": "GOODNOW COLD AND FLU DAY RELIEF COLD AND FLU NIGHT RELIEF (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE) KIT [GOBRANDS, INC]",
"spl_version": "1",
"published_date": "2025-11-19"
}
},
"productid": "82501-0604_97b525ac-bdf4-453d-91a3-eeb7f5a1f069",
"productndc": "82501-0604",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "072096",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Dec 8, 1987"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "GOODNOW PAIN RELIEF",
"active_ingred_unit": "mg/1",
"application_number": "ANDA072096",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20251023",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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