DRY IDEA ADVANCEDDRY ANTIPERSPIRANT UNSCENTED- aluminum zirconium pentachlorohydrex gly liquid 
Henkel Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Aluminum Zirconium Pentachlorohydrex Gly 16.3%

USE....Reduces underarm perspiration - Extra effective

Warnings...For external use only.

Do not use on broken skin.

Stop use and ask a doctor is rash or irritation occurs.

Keep out of reach of children.  If swallowed, get medical help or contact a poison control center right away.

Ask a doctor before use if you have kidney disease.

Directions:  Shake well.  Apply to underarms only.

Inactive Ingredients;  Cyclomethicone, Disteardimonium Hectorite, Propylene Carbonate, Gossypium Herbaceum (Cotton) Seed Oil, Tocopheryl Acetate (Vitamin E Acetate), Isopropyl Myristate, Fragrance, Zea Mays (Corn) Starch.

Questions: 1-800-258-DIAL

2009 Distributed By The Dial Corporation, A Henkel Company, Scottsdale, AZ 85255.  The distinctive design and elements of this package are proprietary and owned by the Dial Corporation, A Henkel Company.

DIRECTIONS: Shake well. Apply to underarms only.

DI_Unsc_New

DRY IDEA ADVANCEDDRY ANTIPERSPIRANT UNSCENTED 
aluminum zirconium pentachlorohydrex gly liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-981
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY (UNII: 94703016SM) (ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY - UNII:94703016SM) ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY16 g  in 96.1 mL
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
TOCOPHEROL (UNII: R0ZB2556P8)  
LEVANT COTTONSEED OIL (UNII: N5CFT140R8)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-981-0196.1 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/16/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM01906/14/201112/01/2022
Labeler - Henkel Corporation (080887708)
Establishment
NameAddressID/FEIBusiness Operations
KDC/ONE Development Corporation, Inc204006464manufacture(54340-981) , analysis(54340-981) , label(54340-981) , pack(54340-981)

Revised: 2/2023
 
Henkel Corporation