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DG BODY ANTIBACTERIAL by DOLGENCORP INC.

Medically reviewed on May 4, 2018

Dosage form: liquid
Ingredients: TRICLOSAN 0.15mL in 100mL
Labeler: DOLGENCORP INC.
NDC Code: 55910-296

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 0.15%

PURPOSE

ANTIBACTERIAL

USES

FOR HAND WASHING TO DECREASE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

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

STOP USE AND ASK A DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS MORE THAN 7 DAYS.

KEEP OUT OF REACH OF CHILDREN

IF ACCIDENTALLY INGESTED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

USE AS A REFILL FOR A PUMP DISPENSING BOTTLE. FROM PUMP BOTTLE, SQUEEZE A SMALL AMOUNT ONTO WET HANDS, LATHER INTO RICH FOAM AND RINSE WELL.

INACTIVE INGREDIENTS

WATER (AQUA), SODIUM C14-16 OLEFIN SULFONATE, LAURAMIDE DEA, SODIUM CHLORIDE, COCAMIDOPROPYL BETAINE, FRAGRANCE (PARFUM), CITRIC ACID, DMDM HYDANTOIN, GLYCERIN, TETRASODIUM EDTA, POLYQUATERNIUM-7, HYDROLYZED SILK PROTEIN, ALOE BARBADENSIS LEAF JUICE, RED 40 (CI 16035), YELLOW 5 (CI 19140), RED 33 (CI 17200).

LABEL COPY

DG BODY  ANTIBACTERIAL
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-296
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.15 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM C14-16 OLEFIN SULFONATE 
LAURIC DIETHANOLAMIDE 
SODIUM CHLORIDE 
COCAMIDOPROPYL BETAINE 
CITRIC ACID MONOHYDRATE 
DMDM HYDANTOIN 
GLYCERIN 
EDETATE SODIUM 
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) 
SILK, ACID HYDROLYZED (1000 MW) 
ALOE VERA LEAF 
FD&C RED NO. 40 
FD&C YELLOW NO. 5 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:55910-296-401180 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/02/2012
Labeler - DOLGENCORP INC. (068331990)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

 
DOLGENCORP INC.

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Further information

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

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