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United States · US · US:63941-245_28729f2d-cd7e-c174-e063-6394a90ac876
All Day Pain Relief
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerVALU MERCHANDISERS COMPANY
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1163941245011 BOTTLE, PLASTIC in 1 CARTON (63941-245-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
- ndc1163941245021 BOTTLE, PLASTIC in 1 CARTON (63941-245-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
- ndc1163941245031 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A079096
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9TN87S3A3C",
"rxcui": "142442",
"inchikey": "CDBRNDSHEYLDJV-FVGYRXGTSA-M",
"display_name": "NAPROXEN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"8889af37-8345-4358-994d-7d8b847f4874": {
"match": "brand_token",
"title": "ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [HYVEE INC]",
"spl_version": "6",
"published_date": "2026-05-13"
}
},
"productid": "63941-245_28729f2d-cd7e-c174-e063-6394a90ac876",
"productndc": "63941-245",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "079096",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Dec 16, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "All Day Pain Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA079096",
"marketing_category": "ANDA",
"nonproprietary_name": "NAPROXEN SODIUM",
"start_marketing_date": "20100519",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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