🇺🇸
United States · US · US:0363-2264_81c4f94d-6f5e-4e69-940b-b94b3533963c
ALL NIGHT PAIN RELIEF PM
Orange BookUNIISPLATC D04AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWalgreen Company
CountryUS (United States)
ATC codeD04AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1103632264271 BOTTLE in 1 CARTON (0363-2264-27) / 80 TABLET, FILM COATED in 1 BOTTLE (0363-2264-80)
Annotations
UNII (FDA Substance ID)
TC2D6JAD40
DIPHENHYDRAMINE HYDROCHLORIDE
RxCUI 1362
Orange Book
A208499
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "TC2D6JAD40",
"rxcui": "1362",
"inchikey": "PCHPORCSPXIHLZ-UHFFFAOYSA-N",
"display_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"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": "0363-2264_81c4f94d-6f5e-4e69-940b-b94b3533963c",
"productndc": "0363-2264",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "208499",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "25MG;220MG",
"product_no": "001",
"approval_date": "May 10, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM",
"proprietary_name": "ALL NIGHT PAIN RELIEF PM",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA208499",
"marketing_category": "ANDA",
"nonproprietary_name": "diphenhydramine hydrochloride, naproxen sodium",
"start_marketing_date": "20260427",
"active_numerator_strength": "25; 220"
}Related drugs
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