Home NDC 82699-201 Dry Idea Advanced Dry Antiperspirant Roll-On, Powder Fresh
Product NDC 82699-201
11-digit product format 826990201
Labeler code 82699
Product ID 82699-201_4979046c-2d35-0e20-e063-6294a90a58dd
Type HUMAN OTC DRUG
Nonproprietary name Dry Idea Advanced Dry Antiperspirant Roll-On, Powder Fresh
Dosage form LIQUID
Route TOPICAL
Labeler Thriving Brands LLC
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-31
Substance ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY
Active strength 16.3 g/16.3g
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 Dry Idea Advanced Dry Antiperspirant Roll-On, Powder Fresh
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY 16.3 g/16.3g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 94703016SM 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 82699-201-03 Dry Idea Advanced Dry Antiperspirant Roll-On, Powder Fresh 96.1 g in 1 BOTTLE, WITH APPLICATOR LIQUID 96.1 4 82699-201-04 Dry Idea Advanced Dry Antiperspirant Roll-On, Powder Fresh 576.6 g in 1 PACKAGE LIQUID 576.6 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82699-201 DRY IDEA ADVANCED DRY ANTIPERSPIRANT ROLL-ON, POWDER FRESH LIQUID [THRIVING BRANDS LLC] 3 Current NDC, 2 package rows 20241219_f8335133-0299-b899-e053-6394a90a3837.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 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 82699-201-03 82699020103 96.1 g in 1 BOTTLE, WITH APPLICATOR (82699-201-03) 96.1 g 2023-03-31 No No Current 82699-201-04 82699020104 576.6 g in 1 PACKAGE (82699-201-04) 576.6 g 2023-09-28 No No Current