vicks zzzquil night pain

Generic: diphenhydramine hydrochloride and acetaminophen

Labeler: the procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name vicks zzzquil night pain
Generic Name diphenhydramine hydrochloride and acetaminophen
Labeler the procter & gamble manufacturing company
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 37000-974
Product ID 37000-974_4407b4f3-f7a5-d59c-e063-6394a90aba2d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M010
Listing Expiration 2026-12-31
Marketing Start 2020-06-01

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 37000974
Hyphenated Format 37000-974

Supplemental Identifiers

RxCUI
1092189
UPC
0323900041400
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 vicks zzzquil night pain (source: ndc)
Generic Name diphenhydramine hydrochloride and acetaminophen (source: ndc)
Application Number M010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (37000-974-60) / 60 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (1)

37000-974-60 1 BOTTLE in 1 CARTON (37000-974-60) / 60 TABLET, COATED in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

Vicks ZzzQuil Night Pain ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4407b4f3-f7a5-d59c-e063-6394a90aba2d", "openfda": {"upc": ["0323900041400"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["a7cf8e2e-7aac-a1fa-e053-2a95a90a561a"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37000-974-60)  / 60 TABLET, COATED in 1 BOTTLE", "package_ndc": "37000-974-60", "marketing_start_date": "20200601"}], "brand_name": "Vicks ZzzQuil Night Pain", "product_id": "37000-974_4407b4f3-f7a5-d59c-e063-6394a90aba2d", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37000-974", "generic_name": "Diphenhydramine Hydrochloride and Acetaminophen", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks ZzzQuil", "brand_name_suffix": "Night Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}