Home NDC 64942-1578 Dove
Product NDC 64942-1578
11-digit product format 649421578
Labeler code 64942
Product ID 64942-1578_253bd708-f288-aecc-e063-6294a90a382d
Type HUMAN OTC DRUG
Nonproprietary name Powder Roll-On AntiPerspirant Deodorant
Dosage form LIQUID
Route TOPICAL
Labeler Conopco Inc. d/b/a/ Unilever
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-10-30
Substance ALUMINUM CHLOROHYDRATE
Active strength 22 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 64942-1578 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 64942-1578 64942-1578-1 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
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 Dove
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 22 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination HPN8MZW13M Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64942-1578-1 Dove 74 mL in 1 CONTAINER LIQUID 74 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64942-1578 DOVE (POWDER ROLL-ON ANTIPERSPIRANT DEODORANT) LIQUID [CONOPCO INC. D/B/A/ UNILEVER] 5 Current NDC, Legacy NDC, 1 package rows 20241027_69749de7-cae0-f339-e053-2a91aa0a3339.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 2 of 73 · 1,450 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 64942-1578-1 64942157801 74 mL in 1 CONTAINER (64942-1578-1) 74 ml 2020-10-30 0000-00-00 No No Current