Home NDC 57337-108 Antiperspirant Dry 1.6 oz Lady
Product NDC 57337-108
11-digit product format 573370108
Labeler code 57337
Product ID 57337-108_2e00fe70-64da-f6e7-e063-6294a90a5f5e
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chlorohydrate
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler Rejoice International Inc.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-13
Substance ALUMINUM CHLOROHYDRATE
Active strength 23.3 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product 57337-108 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 57337-108 57337-108-01 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…
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 Antiperspirant Dry 1.6 oz Lady
Brand name suffix Antiperspirant
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 23.3 g/100g
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 57337-108-01 Antiperspirant Dry 1.6 oz LadyAntiperspirant 45 g in 1 BOTTLE, SPRAY AEROSOL, SPRAY 45 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57337-108 ANTIPERSPIRANT DRY 1.6 OZ LADY ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [REJOICE INTERNATIONAL INC.] 5 Current NDC, Legacy NDC, 1 package rows 20250215_a1b37ad3-a4d6-8d92-e053-2a95a90a7747.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 57337-108-01 57337010801 45 g in 1 BOTTLE, SPRAY (57337-108-01) 45 g 2020-01-13 0000-00-00 No No Current