Home NDC 63029-656-16 GOODYS PM
Product NDC 63029-656
Requested package NDC 63029-656-16
11-digit product format 630290656
Labeler code 63029
Product ID 63029-656_ada25630-e145-4866-b173-435441e2688a
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen and Diphenhydramine Citrate
Dosage form POWDER
Route ORAL
Labeler Medtech Products Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-09-01
Substance ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE
Active strength 500; 38 mg/1; mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base GOODYS PM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 DIPHENHYDRAMINE CITRATE 38 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup 4OD433S209 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1297947 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63029-656-06 GOODYS PM 6 in 1 CARTON POWDER 6 5 63029-656-16 GOODYS PM 16 in 1 CARTON POWDER 16 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63029-656 GOODYS PM (ACETAMINOPHEN AND DIPHENHYDRAMINE CITRATE) POWDER [MEDTECH PRODUCTS INC.] 5 Current NDC, Legacy NDC, 2 package rows 20241101_db5d6c2b-688e-4e88-a42d-0fa2b0d8140b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63029-656-16 63029065616 16 POWDER in 1 CARTON (63029-656-16) 16 powder 2013-09-01 0000-00-00 No No Current