Home NDC 63029-664 GOODYS
Product NDC 63029-664
11-digit product format 630290664
Labeler code 63029
Product ID 63029-664_342847d3-d02e-430a-b1d2-31a13ffd551c
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen, aspirin, and caffeine
Dosage form POWDER
Route ORAL
Labeler Medtech Products Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-08-01
Substance CAFFEINE; ACETAMINOPHEN; ASPIRIN
Active strength 65; 325; 500 mg/1; mg/1; mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
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
Brand name suffix Extra Strength Headache Mixed Fruit Blast
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAFFEINE 65 mg/1 ACETAMINOPHEN 325 mg/1 ASPIRIN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3G6A5W338E Internal UNII lookup 362O9ITL9D Internal UNII lookup R16CO5Y76E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 692836 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63029-664-04 GOODYSExtra Strength Headache Mixed Fruit Blast 4 in 1 CARTON POWDER 4 5 63029-664-24 GOODYSExtra Strength Headache Mixed Fruit Blast 24 in 1 CARTON POWDER 24 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63029-664 GOODYS EXTRA STRENGTH HEADACHE MIXED FRUIT BLAST (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 4 Current NDC, Legacy NDC, 2 package rows 20241116_6cb758bf-5a50-46bb-96e7-65b810b12de0.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 63029-664-04 63029066404 4 POWDER in 1 CARTON (63029-664-04) 4 powder 2015-08-01 0000-00-00 No No Current 63029-664-24 63029066424 24 POWDER in 1 CARTON (63029-664-24) 24 powder 2015-08-01 0000-00-00 No No Current