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Ban Roll-On Antiperspirant Deodorant Regular

Dosage form: liquid
Ingredients: ALUMINUM CHLOROHYDRATE 20g in 103mL
Labeler: Kao Brands Company
NDC Code: 10596-336

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 Regular

DRUG FACTS

Active Ingredients

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 medial 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, SANTALUM ALBUM (SANDALWOOD) EXTRACT, PHELLODENDRON AMURENSE BARK EXTRACT, HORDEUM DISTICHON (BARLEY) EXTRACT, SODIUM SILVER ALUMINUM SILICATE, FRAGRANCE, DISODIUM EDTA, BHT.

Distributed by Kao Brands Company, Cincinnati, OH

45214 Copyright 2011 Reg. U.S. Pat. and Tm. Off. Made in Canada

1-866-226-3363 www.feelbanfresh.com 

Principal Display Panel - 103mL Bottle Label

ban

regular

ROLL-ON

ANTIPERSPIRANT DEODORANT

3.5 FL OZ (103 mL)

BAN  ROLL-ON ANTIPERSPIRANT DEODORANT REGULAR
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10596-336
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 
BUTYLATED HYDROXYTOLUENE 
Packaging
#Item CodePackage Description
1NDC:10596-336-35103 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 Brands Company (004251617)

Revised: 01/2012
Document Id: cd2f8d19-1aa4-4347-9dbf-9a0f4eabd19d
Set id: 1f76588b-e2ea-43b5-ae07-29e290df001d
Version: 1
Effective Time: 20120101
 
Kao Brands Company

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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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