BAN ROLL-ON ANTIPERSPIRANT DEODORANT POWDER FRESH- aluminum chlorohydrate liquid 
Kao USA Inc.

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.

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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.bandeodorant.com

BAN is a trademark of Kao Corp.

Dist. by Kao USA Inc. Cincinnati, OH 45214

©2021 Made in Canada

44 ML PACKAGE

ban

powder fresh
INVISIBLE ROLL-ON

CRUELTY FREE • PARABEN FREE • DYE FREE

1.5 FL OZ (44 mL)

10596-337-15-UPDATED

103 mL PACKAGE

ban

powder fresh
INVISIBLE ROLL-ON

CRUELTY FREE • PARABEN FREE • DYE FREE

3.5 FL OZ (103 mL)

10596-337-35-UPDATED

VALUE PACK

VALUE PACK

2X THE BAN PROTECTION

CRUELTY FREE • PARABEN FREE • DYE FREE

ANTIPERSPIRANT DEODORANT

2 - NET WT 3.5 FL OZ (103 mL)

10596-337-70-UPDATED

BAN  ROLL-ON ANTIPERSPIRANT DEODORANT POWDER FRESH
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10596-337
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20 g  in 103 mL
Inactive Ingredients
Ingredient NameStrength
SUNFLOWER OIL (UNII: 3W1JG795YI)  
PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG)  
WATER (UNII: 059QF0KO0R)  
STEARETH-2 (UNII: V56DFE46J5)  
STEARETH-20 (UNII: L0Q8IK9E08)  
SANDALWOOD (UNII: 3641YW25N2)  
PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)  
BARLEY (UNII: 5PWM7YLI7R)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10596-337-35103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/01/2012
2NDC:10596-337-702 in 1 PACKAGE09/12/2016
2103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
3NDC:10596-337-1544 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/08/2016
4NDC:10596-337-144 in 1 PACKAGE08/24/2020
4103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/01/2012
Labeler - Kao USA Inc. (004251617)

Revised: 3/2023
Document Id: f7f82fb3-852e-f261-e053-6394a90af525
Set id: b99e8972-24e6-4f01-80f5-d071bbab8d30
Version: 9
Effective Time: 20230328
 
Kao USA Inc.