acetaminophen diphenhydramine hcl

Generic: acetaminophen diphenhydramine hcl

Labeler: better living brands llc.
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 better living brands llc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
BETTER LIVING BRANDS LLC.

Identifiers & Regulatory

Product NDC 21130-354
Product ID 21130-354_463f0f6c-a15d-37d7-e063-6394a90a4c6c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-12-12

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 21130354
Hyphenated Format 21130-354

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 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
  • 20 TABLET in 1 BOTTLE (21130-354-02)
  • 80 TABLET in 1 BOTTLE (21130-354-08)
source: ndc

Packages (2)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "463f0f6c-a15d-37d7-e063-6394a90a4c6c", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["ac0f8d5c-d200-1156-e053-2a95a90aece6"], "manufacturer_name": ["BETTER LIVING BRANDS LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (21130-354-02)", "package_ndc": "21130-354-02", "marketing_start_date": "20221212"}, {"sample": false, "description": "80 TABLET in 1 BOTTLE (21130-354-08)", "package_ndc": "21130-354-08", "marketing_start_date": "20221212"}], "brand_name": "Acetaminophen Diphenhydramine HCl", "product_id": "21130-354_463f0f6c-a15d-37d7-e063-6394a90a4c6c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "21130-354", "generic_name": "Acetaminophen Diphenhydramine HCl", "labeler_name": "BETTER LIVING BRANDS LLC.", "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": "20221212", "listing_expiration_date": "20261231"}