counteract pm

Generic: acetaminophen and diphenhydramine

Labeler: melaleuca, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name counteract pm
Generic Name acetaminophen and diphenhydramine
Labeler melaleuca, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Melaleuca, Inc.

Identifiers & Regulatory

Product NDC 54473-304
Product ID 54473-304_7fbf2b51-9097-0a1f-e053-2991aa0a6aa1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part343
Listing Expiration 2026-12-31
Marketing Start 2016-05-02

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 54473304
Hyphenated Format 54473-304

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 counteract pm (source: ndc)
Generic Name acetaminophen and diphenhydramine (source: ndc)
Application Number part343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 BOX (54473-304-01) / 50 TABLET in 1 BOTTLE (54473-304-50)
source: ndc

Packages (1)

54473-304-01 1 BOTTLE in 1 BOX (54473-304-01) / 50 TABLET in 1 BOTTLE (54473-304-50)

Ingredients (2)

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

Linked Drug Pages (1)

CounterAct PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7fbf2b51-9097-0a1f-e053-2991aa0a6aa1", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["7f9a0062-0e86-1deb-e053-2a91aa0a9188"], "manufacturer_name": ["Melaleuca, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (54473-304-01)  / 50 TABLET in 1 BOTTLE (54473-304-50)", "package_ndc": "54473-304-01", "marketing_start_date": "20160502"}], "brand_name": "CounterAct PM", "product_id": "54473-304_7fbf2b51-9097-0a1f-e053-2991aa0a6aa1", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "54473-304", "generic_name": "Acetaminophen and Diphenhydramine", "labeler_name": "Melaleuca, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CounterAct", "brand_name_suffix": "PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20160502", "listing_expiration_date": "20261231"}