acetaminophen, diphenhydramine hcl

Generic: acetaminophen, diphenhydramine hcl

Labeler: cvs pharmacy, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen, diphenhydramine hcl
Generic Name acetaminophen, diphenhydramine hcl
Labeler cvs pharmacy, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
CVS Pharmacy, Inc.

Identifiers & Regulatory

Product NDC 69842-572
Product ID 69842-572_374dc81d-eab9-51f1-e063-6294a90ab12f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2018-07-23

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 69842572
Hyphenated Format 69842-572

Supplemental Identifiers

RxCUI
1092189
UPC
0050428163900
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 acetaminophen, diphenhydramine hcl (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl (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 (69842-572-02) / 225 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (69842-572-08) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (69842-572-12) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 150 TABLET, FILM COATED in 1 BOTTLE (69842-572-29)
source: ndc

Packages (4)

69842-572-02 1 BOTTLE in 1 CARTON (69842-572-02) / 225 TABLET, FILM COATED in 1 BOTTLE 69842-572-08 1 BOTTLE in 1 CARTON (69842-572-08) / 24 TABLET, FILM COATED in 1 BOTTLE 69842-572-12 1 BOTTLE in 1 CARTON (69842-572-12) / 100 TABLET, FILM COATED in 1 BOTTLE 69842-572-29 150 TABLET, FILM COATED in 1 BOTTLE (69842-572-29)

Ingredients (2)

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

Linked Drug Pages (1)

ACETAMINOPHEN, DIPHENHYDRAMINE HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "374dc81d-eab9-51f1-e063-6294a90ab12f", "openfda": {"upc": ["0050428163900"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["6df9a638-09dd-166f-e053-2991aa0a8dd0"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-572-02)  / 225 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-572-02", "marketing_start_date": "20230202"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-572-08)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-572-08", "marketing_start_date": "20180723"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-572-12)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-572-12", "marketing_start_date": "20180723"}, {"sample": false, "description": "150 TABLET, FILM COATED in 1 BOTTLE (69842-572-29)", "package_ndc": "69842-572-29", "marketing_start_date": "20180723"}], "brand_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HCL", "product_id": "69842-572_374dc81d-eab9-51f1-e063-6294a90ab12f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69842-572", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HCL", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN, DIPHENHYDRAMINE HCL", "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": "20180723", "listing_expiration_date": "20261231"}