ANTIBACTERIAL FOAMING HAND SP CUCUMBER AND MELON

Dosage form: liquid
Ingredients: TRICLOSAN 0.6mL in 100mL
Labeler: AMERICAN SALES COMPANY
NDC Code: 41520-167

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.

DRUG FACTS

ACTIVE INGREDIENT

TRICLOSAN 0.60 PERCENT

PURPOSE

ANTIBACTERIAL

USES

FOR HAND WASHING TO REDUCE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES.  IF CONTACT OCCURS, RINSE EYES THROUGHLY WITH WATER.

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION AND REDNESS DEVELOP.

DIRECTIONS

PUMP ONTO DRY HANDS, WORK INTO LATHER AND RINSE THOROUGHLY.

OTHER INFORMATIONSTORE AT ROOM TEMPERATURE.

INACTIVE INGREDIENTS

WATER, SODIUM XYLENESULFONATE,  DIPROPYLENE GLYCOL,AMMONIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, FRAGRANCE,  DISODIUM PHOSPHATE, CITRIC ACID, BLUE 1, YELLOW 5, RED 40.

ANTIBACTERIAL FOAMING HAND SP CUCUMBER AND MELON 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41520-167
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.6 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM XYLENESULFONATE 
DIPROPYLENE GLYCOL 
AMMONIUM LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
SODIUM PHOSPHATE, DIBASIC, DIHYDRATE 
CITRIC ACID MONOHYDRATE 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
FD&C RED NO. 40 
Packaging
#Item CodePackage Description
1NDC:41520-167-08221 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/24/2011
Labeler - AMERICAN SALES COMPANY (809183973)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

Revised: 05/2011
 
AMERICAN SALES 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 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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