Home NDC 57337-183 3.5OZ WOMENS DRY WHITE LILY
Product NDC 57337-183
11-digit product format 573370183
Labeler code 57337
Product ID 57337-183_3f747b46-58ac-49e5-e063-6394a90a468d
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chlorohydrate
Dosage form SPRAY
Route TOPICAL
Labeler Rejoice International Corp.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-23
Substance ALUMINUM CHLOROHYDRATE
Active strength 24.5 g/100g
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 3.5OZ WOMENS DRY WHITE LILY
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 24.5 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57337-183-01 3.5OZ WOMENS DRY WHITE LILY 99 g in 1 CAN SPRAY 99 1
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 70 of 73 · 1,450 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 57337-183-01 57337018301 99 g in 1 CAN (57337-183-01) 99 g 2025-09-23 No No Current