Skip to Content

3 in 1 Antibacterial Hair and Body Wash

Medically reviewed on February 14, 2018

Dosage form: solution
Ingredients: TRICLOSAN 11.7g in 100mL
Labeler: Kutol Products Company, Inc.
NDC Code: 50865-076

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.

3 in 1 Antibacterial Hair and Body Wash

Triclosan 0.3% w/w.....Antibacterial Agent

Water, Ammonium Lauryl Sulfate, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Hydroxysultaine, Disodium Cocamido MIPA-Sulfosuccinate, Glycerin, Fragrance, Citric Acid, Tetrasodium EDTA, DMDM Hydantoin, Blue 1.

For handwashing to help reduce bacteria on the skin

For external use only.

Avoid contact with eyes. If eye contact occurs, flush eyes with water.

Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.

Keep out of reach of children. If swallowed, contact a physician or poison control center.

Apply to hair or body. Work into a rich lather. Massage hair and body completely for at least 30 seconds. Rinse thoroughly. Dry completely.

For handwashing to help reduce bacteria on the skin.

Avoid contact with eyes. If eye contact occurs, flush eyes with water.

Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.

Keep out of reach of children. If swallowed, contact a physician or poison control center.

Keep out of reach of children. If swallowed, contact a physician or poison control center.

50865-076-41.jpg

3 IN 1 ANTIBACTERIAL HAIR AND BODY WASH 
3 in 1 antibacterial hair and body wash solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50865-076
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN11.7 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
AMMONIUM LAURYL SULFATE 
SODIUM LAURETH SULFATE 
COCAMIDOPROPYL HYDROXYSULTAINE 
GLYCERIN 
ANHYDROUS CITRIC ACID 
ISOSTEARAMIDOPROPYL MORPHOLINE LACTATE 
DMDM HYDANTOIN 
EDETATE SODIUM 
SODIUM CHLORIDE 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:50865-076-073785 mL in 1 JUG
2NDC:50865-076-093785 mL in 1 BOTTLE, PLASTIC
3NDC:50865-076-361000 mL in 1 BOTTLE, PLASTIC
4NDC:50865-076-411000 mL in 1 BAG
5NDC:50865-076-672000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/06/2013
Labeler - Kutol Products Company, Inc. (004236139)
Establishment
NameAddressID/FEIOperations
Kutol Products Company, Inc.004236139manufacture(50865-076), analysis(50865-076), label(50865-076), pack(50865-076)

 
Kutol Products Company, Inc.

Further information

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

Hide