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 LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 1000 mg/30mL, diphenhydramine hydrochloride 50 mg/30mL

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 69423-985
Product ID 69423-985_402e4f97-f5d4-8d35-e063-6394a90aa903
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M010
Listing Expiration 2026-12-31
Marketing Start 2023-03-03

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 69423985
Hyphenated Format 69423-985

Supplemental Identifiers

RxCUI
1092373
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
  • 1000 mg/30mL
  • 50 mg/30mL
source: ndc
Packaging
  • 2 BOTTLE in 1 CARTON (69423-985-02) / 354 mL in 1 BOTTLE
  • 354 mL in 1 BOTTLE (69423-985-12)
source: ndc

Packages (2)

69423-985-02 2 BOTTLE in 1 CARTON (69423-985-02) / 354 mL in 1 BOTTLE 69423-985-12 354 mL in 1 BOTTLE (69423-985-12)

Ingredients (2)

acetaminophen (1000 mg/30mL) diphenhydramine hydrochloride (50 mg/30mL)

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": "402e4f97-f5d4-8d35-e063-6394a90aa903", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092373"], "spl_set_id": ["f3bb75e8-3d43-f91e-e053-2a95a90a584d"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (69423-985-02)  / 354 mL in 1 BOTTLE", "package_ndc": "69423-985-02", "marketing_start_date": "20230303"}, {"sample": false, "description": "354 mL in 1 BOTTLE (69423-985-12)", "package_ndc": "69423-985-12", "marketing_start_date": "20230303"}], "brand_name": "Vicks ZzzQuil Night Pain", "product_id": "69423-985_402e4f97-f5d4-8d35-e063-6394a90aa903", "dosage_form": "LIQUID", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69423-985", "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": "1000 mg/30mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/30mL"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230303", "listing_expiration_date": "20261231"}