tylenol pm extra strength, cvp health

Generic: acetaminophen and diphenhydramine hydrochloride

Labeler: lil' drug store products, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tylenol pm extra strength, cvp health
Generic Name acetaminophen and diphenhydramine hydrochloride
Labeler lil' drug store products, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Lil' Drug Store Products, Inc.

Identifiers & Regulatory

Product NDC 66715-6517
Product ID 66715-6517_459f9062-e920-d327-e063-6394a90acc1d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-05-06

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 667156517
Hyphenated Format 66715-6517

Supplemental Identifiers

RxCUI
1092189 1092378
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 tylenol pm extra strength, cvp health (source: ndc)
Generic Name acetaminophen and diphenhydramine hydrochloride (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 2 POUCH in 1 CARTON (66715-6517-2) / 2 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (1)

66715-6517-2 2 POUCH in 1 CARTON (66715-6517-2) / 2 TABLET, FILM COATED in 1 POUCH

Ingredients (2)

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

Linked Drug Pages (1)

Tylenol PM Extra Strength, CVP HEALTH, Lil Drug Store Tylenol PM Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459f9062-e920-d327-e063-6394a90acc1d", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189", "1092378"], "spl_set_id": ["643371f2-e330-441e-8932-b3aec4b179d2"], "manufacturer_name": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 CARTON (66715-6517-2)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-6517-2", "marketing_start_date": "20220506"}], "brand_name": "Tylenol PM Extra Strength, CVP HEALTH", "product_id": "66715-6517_459f9062-e920-d327-e063-6394a90acc1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "66715-6517", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tylenol PM Extra Strength, CVP HEALTH", "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": "20220506", "listing_expiration_date": "20261231"}