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Ban Roll-On Antiperspirant Deodorant Powder Fresh

Dosage form: liquid
Ingredients: ALUMINUM CHLOROHYDRATE 20g in 103mL
Labeler: Kao USA Inc.
NDC Code: 10596-337

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.

Ban Roll-On Antiperspirant Deodorant Powder Fresh

Drug Facts

Active ingredient

Aluminum chlorohydrate 18%

Purpose

Antiperspirant

Use

reduces underarm perspiration

Warnings

For external use only

Do not use on broken skin

Stop use if rash or irritation occurs

Ask a doctor before use if you have kidney disease

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

Directions

apply to underarms only

Other information

store at room temperature

Inactive ingredients

water, PPG-11 stearyl ether, steareth-2, steareth-20, fragrance, disodium EDTA, helianthus annus (sunflower) seed oil, phellodendron amurense bark extract, hordeum distichon (barley) extract, santalum album (sandalwood) extract

Questions? 1-866-226-3363

www.feelbanfresh.com

Dist. by Kao USA Inc. Cincinnati, OH 45214

© 2016 Reg. U.S. Pat. and Tm. Off.

Made in Canada


ban®

powder fresh
ROLL-ON

ANTIPERSPIRANT DEODORANT

3.5 FL OZ (103 mL)

BAN  ROLL-ON ANTIPERSPIRANT DEODORANT POWDER FRESH
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10596-337
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE20 g  in 103 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
STEARETH-2 
STEARETH-20 
SANDALWOOD 
PHELLODENDRON AMURENSE BARK 
BARLEY 
EDETATE DISODIUM 
PPG-11 STEARYL ETHER 
SUNFLOWER OIL 
Packaging
#Item CodePackage Description
1NDC:10596-337-35103 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/01/2012
Labeler - Kao USA Inc. (004251617)

Revised: 05/2016
 
Kao USA Inc.

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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