Dry Idea Advanced Dry-Powder Fresh

Dosage form: liquid
Ingredients: Aluminum Zirconium Pentachlorohydrex gly 16.3g in 100mL
Labeler: The Dial Corporation
NDC Code: 54340-005

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

  • Reduces underarm perspiration
  • Extra effective


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









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DRY IDEA ADVANCED DRY-POWDER FRESH 
aluminum zirconium pentachlorohydrex gly liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-005
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Zirconium Pentachlorohydrex gly (Aluminum Zirconium Pentachlorohydrex Gly) Aluminum Zirconium Pentachlorohydrex Gly16.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Cyclomethicone74.5 g  in 100 mL
Propylene Carbonate1 g  in 100 mL
.ALPHA.-TOCOPHEROL ACETATE, D-0.1 g  in 100 mL
STEARYL MYRISTATE0.1 g  in 100 mL
Bentonite4.1 g  in 100 mL
Packaging
#Item CodePackage Description
1NDC:54340-005-1212 BOTTLE, PLASTIC (BOTTLE) 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/FEIOperations
Diversapack of Monroe832713825pack, manufacture

Revised: 10/2011
 
The Dial Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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