Home NDC 87119-001 MDS Roll-On Anti-Perspirant
Product NDC 87119-001
11-digit product format 871190001
Labeler code 87119
Product ID 87119-001_4340f1c6-a2eb-b885-e063-6394a90a0cae
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chlorohydrate
Dosage form CREAM
Route TOPICAL
Labeler MDS GLOBAL FZE
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-23
Substance ALUMINUM CHLOROHYDRATE ANHYDROUS
Active strength 15.4 g/100mL
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 MDS Roll-On Anti-Perspirant
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE ANHYDROUS 15.4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 407PSC3OC7 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 87119-001-01 MDS Roll-On Anti-Perspirant 50 mL in 1 BOTTLE CREAM 50 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 87119-001-01 87119000101 50 mL in 1 BOTTLE (87119-001-01) 50 ml 2025-09-23 No No Current