Home NDC 83711-142 Suave Dry Antiperspirant Deodorant Powder and Petals
Product NDC 83711-142
11-digit product format 837110142
Labeler code 83711
Product ID 83711-142_4df1d1b6-a91d-5522-e063-6394a90ae48c
Type HUMAN OTC DRUG
Nonproprietary name Dry Spray Antiperspirant Deodorant
Dosage form SPRAY
Route TOPICAL
Labeler Suave Brands Co, LLC
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-21
Substance ALUMINUM CHLOROHYDRATE
Active strength 23.3 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 Suave Dry Antiperspirant Deodorant Powder and Petals
Listing expiration 2027-12-31 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83711-142-38 Suave Dry Antiperspirant Deodorant Powder and Petals 107 g in 1 BOTTLE, SPRAY SPRAY 107 4
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 83711-142-38 83711014238 107 g in 1 BOTTLE, SPRAY (83711-142-38) 107 g 2025-10-21 No No Current