goodmeds extra strength pain relief pm

Generic: acetaminophen, diphenhydramine hydrochloride

Labeler: cabinet health p.b.c.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name goodmeds extra strength pain relief pm
Generic Name acetaminophen, diphenhydramine hydrochloride
Labeler cabinet health p.b.c.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Cabinet Health P.B.C.

Identifiers & Regulatory

Product NDC 82725-4124
Product ID 82725-4124_47bb2403-7eb4-0d01-e063-6294a90a2ea7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2025-11-11

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 827254124
Hyphenated Format 82725-4124

Supplemental Identifiers

RxCUI
1092189
UPC
0850069928179
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 goodmeds extra strength pain relief pm (source: ndc)
Generic Name acetaminophen, 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
  • 375 TABLET in 1 BOTTLE (82725-4124-1)
source: ndc

Packages (1)

82725-4124-1 375 TABLET in 1 BOTTLE (82725-4124-1)

Ingredients (2)

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

Linked Drug Pages (1)

Goodmeds Extra Strength Pain Relief PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47bb2403-7eb4-0d01-e063-6294a90a2ea7", "openfda": {"upc": ["0850069928179"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["02c60967-46d7-49b7-82be-bc3c5fd36484"], "manufacturer_name": ["Cabinet Health P.B.C."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "375 TABLET in 1 BOTTLE (82725-4124-1)", "package_ndc": "82725-4124-1", "marketing_start_date": "20251111"}], "brand_name": "Goodmeds Extra Strength Pain Relief PM", "product_id": "82725-4124_47bb2403-7eb4-0d01-e063-6294a90a2ea7", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82725-4124", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "Cabinet Health P.B.C.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Goodmeds Extra Strength Pain Relief 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": "20251111", "listing_expiration_date": "20271231"}