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United States · US · US:56062-748_581830ee-5c9a-40aa-8bf7-c02dcda51e0f
All Day Relief
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPublix Supermarkets, Inc.
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1156062748401 BOTTLE, PLASTIC in 1 BOX (56062-748-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A208363
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": "56062-748_581830ee-5c9a-40aa-8bf7-c02dcda51e0f",
"productndc": "56062-748",
"dosage_form": "CAPSULE, LIQUID FILLED",
"orange_book": {
"appl_no": "208363",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 200MG BASE",
"product_no": "001",
"approval_date": "Mar 15, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "All Day Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA208363",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20190630",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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