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United States · US · US:79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83
All Day Pain Relief
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWALMART INC.
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc117990300520200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)
- ndc117990300525225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)
- ndc117990300527270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)
- ndc11799030059090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A204872
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": "79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83",
"productndc": "79903-005",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "204872",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Jan 23, 2017"
}
],
"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": "ANDA204872",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20201022",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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