goodys pm

Generic: acetaminophen and diphenhydramine citrate

Labeler: medtech products inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name goodys pm
Generic Name acetaminophen and diphenhydramine citrate
Labeler medtech products inc.
Dosage Form POWDER
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine citrate 38 mg/1

Manufacturer
Medtech Products Inc.

Identifiers & Regulatory

Product NDC 63029-656
Product ID 63029-656_ada25630-e145-4866-b173-435441e2688a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2013-09-01

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 63029656
Hyphenated Format 63029-656

Supplemental Identifiers

RxCUI
1297947
UPC
0042037102951
UNII
362O9ITL9D 4OD433S209

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 goodys pm (source: ndc)
Generic Name acetaminophen and diphenhydramine citrate (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 38 mg/1
source: ndc
Packaging
  • 6 POWDER in 1 CARTON (63029-656-06)
  • 16 POWDER in 1 CARTON (63029-656-16)
source: ndc

Packages (2)

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine citrate (38 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ada25630-e145-4866-b173-435441e2688a", "openfda": {"upc": ["0042037102951"], "unii": ["362O9ITL9D", "4OD433S209"], "rxcui": ["1297947"], "spl_set_id": ["db5d6c2b-688e-4e88-a42d-0fa2b0d8140b"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER in 1 CARTON (63029-656-06)", "package_ndc": "63029-656-06", "marketing_start_date": "20130901"}, {"sample": false, "description": "16 POWDER in 1 CARTON (63029-656-16)", "package_ndc": "63029-656-16", "marketing_start_date": "20130901"}], "brand_name": "GOODYS PM", "product_id": "63029-656_ada25630-e145-4866-b173-435441e2688a", "dosage_form": "POWDER", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63029-656", "generic_name": "Acetaminophen and Diphenhydramine Citrate", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GOODYS PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130901", "listing_expiration_date": "20261231"}