Home NDC 63029-662 Goodys Extra Strength
Product NDC 63029-662
11-digit product format 630290662
Labeler code 63029
Product ID 63029-662_a04a69da-506e-415a-9fff-eb75f3002fc6
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Aspirin, and Caffeine
Dosage form POWDER
Route ORAL
Labeler Medtech Products Inc.
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2013-11-01
Marketing end 2023-11-30
Substance ACETAMINOPHEN; ASPIRIN; CAFFEINE
Active strength 260 mg/1; mg/1; mg/1
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 26 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63029-662-01 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 63029-662-01 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 63029-662-01 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 63029-662-01 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 63029-662-01 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 63029-662-01 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 63029-662-01 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 63029-662-01 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 63029-662-01 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 63029-662-01 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 63029-662-01 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 63029-662-01 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 63029-662-01 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 63029-662-01 Goodys Extra Strength 6 in 1 BOX POWDER 6 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2 ASPIRIN ACTIVE INGREDIENT R16CO5Y76E GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2 CAFFEINE ACTIVE INGREDIENT 3G6A5W338E GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2 ASPIRIN ACTIVE MOIETY R16CO5Y76E GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2 CAFFEINE ACTIVE MOIETY 3G6A5W338E GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2 LACTOSE MONOHYDRATE INACTIVE INGREDIENT EWQ57Q8I5X GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2 POTASSIUM INACTIVE INGREDIENT RWP5GA015D GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63029-662 GOODYS EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.] 5 Legacy NDC, 1 package rows 20241101_16d774cc-4247-4bf8-9b5a-c338ffebda3d.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 1 · 1 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 63029-662-01 63029066201 6 POWDER in 1 BOX (63029-662-01) 6 powder 2013-11-01 2023-11-30 No No Current