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United States · US · US:11673-166_ab380f8c-73e9-429c-80d6-05929e72eae4
Up and Up childrens ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1111673166341 BOTTLE in 1 CARTON (11673-166-34) / 237 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A074937
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": {
"51c0a953-93cb-4d0a-b51c-02d9482d1746": {
"match": "brand_token",
"title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
"spl_version": "12",
"published_date": "2026-05-13"
}
},
"productid": "11673-166_ab380f8c-73e9-429c-80d6-05929e72eae4",
"productndc": "11673-166",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "074937",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "100MG/5ML",
"product_no": "001",
"approval_date": "Dec 22, 1998"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Up and Up childrens ibuprofen",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA074937",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20090612",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code G02CC01.
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