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United States · US · US:0363-9608_13aeca7d-1120-844d-e063-6294a90ac3d9
ALL DAY PAIN RELIEF
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWALGREENS
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc11036396080550 TABLET, COATED in 1 BOTTLE (0363-9608-05)
- ndc1103639608091 BOTTLE in 1 CARTON (0363-9608-09) / 90 TABLET, COATED in 1 BOTTLE
- ndc110363960820200 TABLET, COATED in 1 BOTTLE (0363-9608-20)
- ndc110363960827270 TABLET, COATED in 1 BOTTLE (0363-9608-27)
- ndc1103639608421 BOTTLE in 1 CARTON (0363-9608-42) / 24 TABLET, COATED in 1 BOTTLE
- ndc110363960861600 TABLET, COATED in 1 BOTTLE (0363-9608-61)
- ndc11036396089090 TABLET, COATED in 1 BOTTLE (0363-9608-90)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A090545
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": "0363-9608_13aeca7d-1120-844d-e063-6294a90ac3d9",
"productndc": "0363-9608",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "090545",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Mar 16, 2011"
}
],
"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": "ANDA090545",
"marketing_category": "ANDA",
"nonproprietary_name": "NAPROXEN SODIUM",
"start_marketing_date": "20190626",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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