DRY IDEA ADVANCED DRY-POWDER FRESH - aluminum zirconium pentachlorohydrex gly  liquid 
The Dial 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.

----------

Drug Facts

Active  Ingredient Purpose

Aluminum Zirconium Pentacholrohydrex Gly 16.3%.......Antiperspirant

Antiperspirant

Use


Warnings for external use only.

Do not use on broken skin.

Stop use and ask a doctor if

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









image of dry idea-powder fresh label
dryidea-powderfresh.jpg
DRY IDEA ADVANCED DRY-POWDER FRESH 
aluminum zirconium pentachlorohydrex gly liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-005
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 Gly16.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Cyclomethicone (UNII: NMQ347994Z) 74.5 g  in 100 mL
Propylene Carbonate (UNII: 8D08K3S51E) 1 g  in 100 mL
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) 0.1 g  in 100 mL
STEARYL MYRISTATE (UNII: 310RUQ1G0W) 0.1 g  in 100 mL
Bentonite (UNII: A3N5ZCN45C) 4.1 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-005-1212 in 1 BOX
1NDC:54340-005-3296.1 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35010/18/2011
Labeler - The Dial Corporation (070252531)
Establishment
NameAddressID/FEIBusiness Operations
Diversapack of Monroe832713825pack, manufacture

Revised: 10/2011
Document Id: 89f039bf-2ba7-40e0-8376-e18e346cc0b2
Set id: 8de4560e-bd9a-4527-b79b-037219e699a3
Version: 8
Effective Time: 20111018
 
The Dial Corporation