extra strength nite-time pain relief

Generic: 430r walgreens acetaminophen 500 mg,diphenhydramine hcl 25 mg tablet

Labeler: walgreens
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength nite-time pain relief
Generic Name 430r walgreens acetaminophen 500 mg,diphenhydramine hcl 25 mg tablet
Labeler walgreens
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1

Manufacturer
WALGREENS

Identifiers & Regulatory

Product NDC 0363-0715
Product ID 0363-0715_2ceafa1d-d834-3d30-e063-6294a90ac3e5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-10-12

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630715
Hyphenated Format 0363-0715

Supplemental Identifiers

RxCUI
1092189
UNII
362O9ITL9D TC2D6JAD40

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name extra strength nite-time pain relief (source: ndc)
Generic Name 430r walgreens acetaminophen 500 mg,diphenhydramine hcl 25 mg tablet (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-0715-01) / 100 TABLET in 1 BOTTLE
source: ndc

Packages (1)

0363-0715-01 1 BOTTLE in 1 CARTON (0363-0715-01) / 100 TABLET in 1 BOTTLE

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Extra Strength Nite-Time Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2ceafa1d-d834-3d30-e063-6294a90ac3e5", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["c25cff5a-93f5-62aa-e053-2a95a90aa7b4"], "manufacturer_name": ["WALGREENS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0715-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "0363-0715-01", "marketing_start_date": "20211012"}], "brand_name": "Extra Strength Nite-Time Pain Relief", "product_id": "0363-0715_2ceafa1d-d834-3d30-e063-6294a90ac3e5", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-0715", "generic_name": "430R WALGREENS Acetaminophen 500 mg,Diphenhydramine HCl 25 mg Tablet", "labeler_name": "WALGREENS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Nite-Time Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211012", "listing_expiration_date": "20261231"}