pain reliever pm
Generic: acetaminophen, diphenhydramine hcl
Labeler: wr group, inc.Drug Facts
Product Profile
Brand Name
pain reliever pm
Generic Name
acetaminophen, diphenhydramine hcl
Labeler
wr group, inc.
Dosage Form
TABLET, COATED
Routes
Active Ingredients
acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69607-8630
Product ID
69607-8630_a93c6c12-674e-425e-9015-e40fe4b059f6
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2025-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
696078630
Hyphenated Format
69607-8630
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
pain reliever pm (source: ndc)
Generic Name
acetaminophen, diphenhydramine hcl (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
- 25 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 BOX (69607-8630-1) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a93c6c12-674e-425e-9015-e40fe4b059f6", "openfda": {"upc": ["0811079036971"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["8281771c-485c-42a9-9a1c-9a7a4298c5b8"], "manufacturer_name": ["WR Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (69607-8630-1) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "69607-8630-1", "marketing_start_date": "20250228"}], "brand_name": "Pain Reliever PM", "product_id": "69607-8630_a93c6c12-674e-425e-9015-e40fe4b059f6", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69607-8630", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "WR Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever PM", "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": "20250228", "listing_expiration_date": "20261231"}