extra strength nitetime pain relief

Generic: acetaminophen 500 mg,diphenhydramine hydrochloride 25 mg tablet

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

Drug Facts

Product Profile

Brand Name extra strength nitetime pain relief
Generic Name acetaminophen 500 mg,diphenhydramine hydrochloride 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 0363-0714
Product ID 0363-0714_3ac05a52-7cce-2bfb-e063-6394a90a134b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
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 03630714
Hyphenated Format 0363-0714

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 nitetime pain relief (source: ndc)
Generic Name acetaminophen 500 mg,diphenhydramine hydrochloride 25 mg tablet (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-0714-42) / 24 TABLET in 1 BOTTLE
source: ndc

Packages (1)

0363-0714-42 1 BOTTLE in 1 CARTON (0363-0714-42) / 24 TABLET in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

Extra Strength NiteTime Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ac05a52-7cce-2bfb-e063-6394a90a134b", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["c25c75c7-157f-1c0d-e053-2995a90a2e3c"], "manufacturer_name": ["WALGREENS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0714-42)  / 24 TABLET in 1 BOTTLE", "package_ndc": "0363-0714-42", "marketing_start_date": "20211012"}], "brand_name": "Extra Strength NiteTime Pain Relief", "product_id": "0363-0714_3ac05a52-7cce-2bfb-e063-6394a90a134b", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-0714", "generic_name": "Acetaminophen 500 mg,Diphenhydramine Hydrochloride 25 mg Tablet", "labeler_name": "WALGREENS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength NiteTime Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211012", "listing_expiration_date": "20261231"}