Degree Clinical Protection Motion Sense Linen Dry Antiperspirant and Deodorant

Dosage form: stick
Ingredients: Aluminum Zirconium Tetrachlorohydrex GLY 20g in 100g
Labeler: Conopco Inc. d/b/a Unilever
NDC Code: 64942-1208

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.

Degree Clinical Protection Motion Sense Linen Dry antiperspirant deodorant

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (20%)

Purpose
anti-perspirant

Warnings
For external use only

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Uses
▪  reduces underarm wetness
▪  24 hour protection
▪  extra effective

Directions
▪  apply to underarms only
▪  before bed, apply two clicks of product to each underarm

Inactive ingredients
Cyclopentasiloxane
Dimethicone
Paraffin
Microcrystalline Wax
Fragrance (Parfum)
Silica
Caprylic/Capric Triglyceride
Sodium Starch Octenylsuccinate
Dimethicone Crosspolymer
Hydrated silica
Maltodextrin
Gelatin crosspolymer
Hydrolyzed Corn Starch
Cellulose Gum
BHT

Questions?  Call toll-free 1-866-DEGREE1

PDP 2.7 oz

2.7 oz carton
DEGREE  CLINICAL PROTECTION MOTION SENSE LINEN DRY ANTIPERSPIRANT AND DEODORANT
aluminum zirconium tetrachlorohydrex gly stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1208
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Zirconium Tetrachlorohydrex GLY (Aluminum cation) Aluminum Zirconium Tetrachlorohydrex GLY20 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 
DIMETHICONE 
MICROCRYSTALLINE WAX 
SILICON DIOXIDE 
HYDRATED SILICA 
MALTODEXTRIN 
STARCH, CORN 
GELATIN 
CARBOXYMETHYLCELLULOSE SODIUM 
BUTYLATED HYDROXYTOLUENE 
PARAFFIN 
Packaging
#Item CodePackage Description
1NDC:64942-1208-21 CONTAINER (CONTAINER) in 1 CARTON
1NDC:64942-1208-176 g in 1 CONTAINER
2NDC:64942-1208-41 CONTAINER (CONTAINER) in 1 CARTON
2NDC:64942-1208-348 g in 1 CONTAINER
3NDC:64942-1208-61 CONTAINER (CONTAINER) in 1 CARTON
3NDC:64942-1208-514 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35011/01/2011
Labeler - Conopco Inc. d/b/a Unilever (001375088)

Revised: 10/2011
 
Conopco Inc. d/b/a Unilever

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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