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Ban Roll-On Antiperspirant Deodorant Unscented

Medically reviewed by Drugs.com. Last updated on Aug 24, 2020.

Dosage form: liquid
Ingredients: ALUMINUM CHLOROHYDRATE 20g in 103mL
Labeler: Kao USA Inc.
NDC Code: 10596-338

Ban Roll-On Antiperspirant Deodorant Unscented

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, helianthus annuus (sunflower) seed oil, phellodendron amurense bark extract, hordeum distichon (barley) extract, santalum album (sandalwood) extract

Questions? 1-866-226-3363

www.feelbanfresh.com

BAN is a trademark of Kao Corp.

Dist. by Kao USA Inc. Cincinnati, OH 45214

©2016 Made in Canada

ban

unscented
ROLL-ON

ANTIPERSPIRANT

DEODORANT

3.5 FL OZ (103 mL)

BAN  ROLL-ON ANTIPERSPIRANT DEODORANT UNSCENTED
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10596-338
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 
PPG-11 STEARYL ETHER 
SUNFLOWER OIL 
Packaging
#Item CodePackage Description
1NDC:10596-338-35103 mL in 1 BOTTLE, WITH APPLICATOR
2NDC:10596-338-702 BOTTLE, WITH APPLICATOR in 1 PACKAGE
2103 mL in 1 BOTTLE, WITH APPLICATOR
3NDC:10596-338-1544 mL in 1 BOTTLE, WITH APPLICATOR
4NDC:10596-338-113 BOTTLE, WITH APPLICATOR in 1 PACKAGE
4103 mL in 1 BOTTLE, WITH APPLICATOR
5NDC:10596-338-144 BOTTLE, WITH APPLICATOR in 1 PACKAGE
5103 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)

 
Kao USA Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.