Home NDC 64942-1141-4 Dove
Product NDC 64942-1141
Requested package NDC 64942-1141-4
11-digit product format 649421141
Labeler code 64942
Product ID 64942-1141_ef17c871-6af8-53c0-e053-2a95a90acb4b
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Zirconium Tetrachlorohydrex GLY
Dosage form STICK
Route TOPICAL
Labeler Conopco Inc. d/b/a Unilever
Application part350
Marketing category OTC MONOGRAPH FINAL
Marketing start 2020-10-30
Marketing end 0000-00-00
Substance ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Active strength 20 g/100g
NDC exclude flag No
Listing certified through 2023-12-31
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 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2020-06-10 20:45 UTC · source 2020-06-10 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64942-1141-1 DoveClinical Protection Revive Antiperspirant and Deodorant 48 g in 1 CONTAINER STICK 48 9 64942-1141-2 DoveClinical Protection Revive Antiperspirant and Deodorant 1 in 1 CARTON STICK 1 9 64942-1141-3 DoveClinical Protection Revive Antiperspirant and Deodorant 14 g in 1 CONTAINER STICK 14 9 64942-1141-4 DoveClinical Protection Revive Antiperspirant and Deodorant 1 in 1 CARTON STICK 1 9 64942-1141-5 DoveClinical Protection Revive Antiperspirant and Deodorant 62 g in 1 CONTAINER STICK 62 9 64942-1141-6 DoveClinical Protection Revive Antiperspirant and Deodorant 1 in 1 CARTON STICK 1 9 64942-1141-7 DoveClinical Protection Revive Antiperspirant and Deodorant 74 g in 1 CONTAINER STICK 74 9 64942-1141-8 DoveClinical Protection Revive Antiperspirant and Deodorant 1 in 1 CARTON STICK 1 9
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64942-1141 DOVE CLINICAL PROTECTION REVIVE ANTIPERSPIRANT AND DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER] 9 Legacy NDC, 8 package rows 20230328_a330b97d-7134-4f2c-9cba-318808d6c2bc.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 64942-1141-4 64942114104 1 CONTAINER in 1 CARTON (64942-1141-4) > 14 g in 1 CONTAINER (64942-1141-3) 1 container 2020-10-30 0000-00-00 No No Current