FDA.reportPublic FDA data

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

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
IngredientStrength
ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY16.3 g/16.3g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii94703016SM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82699-201-03Dry Idea Advanced Dry Antiperspirant Roll-On, Powder Fresh96.1 g in 1 BOTTLE, WITH APPLICATORLIQUID96.14
82699-201-04Dry Idea Advanced Dry Antiperspirant Roll-On, Powder Fresh576.6 g in 1 PACKAGELIQUID576.64

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82699-201DRY IDEA ADVANCED DRY ANTIPERSPIRANT ROLL-ON, POWDER FRESH LIQUID [THRIVING BRANDS LLC]3Current NDC, 2 package rows20241219_f8335133-0299-b899-e053-6394a90a3837.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82699-201-038269902010396.1 g in 1 BOTTLE, WITH APPLICATOR (82699-201-03) 96.1 g2023-03-31NoNoCurrent
82699-201-0482699020104576.6 g in 1 PACKAGE (82699-201-04) 576.6 g2023-09-28NoNoCurrent