Skip to Content

← See all DG BODY ANTIBACTERIAL brands

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: 55910-294

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

HELPS REDUCE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

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

STOP USING THIS PRODUCT AND ASK A DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

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

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.

OTHER INFORMATION

STORE AT ROOM TEMPERATURE.

INACTIVE INGREDIENTS

WATER (AQUA), SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, SODIUM CHLORIDE, COCAMIDOPROPYL HYDROXYSULTAINE, GLYCERIN, FRAGRANCE (PARFUM), POLYQUATERNIUM-7, PPG-2 HYDROXYETHYL COCO/ISOSTEARAMIDE, DMDM HYDANTOIN, TETRASODIUM EDTA, CITRIC ACID, YELLOW 5 (CI 19140), RED 4 (CI 14700).

LABEL COPY

DG BODY  ANTIBACTERIAL
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-294
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 LAURETH SULFATE 
COCAMIDOPROPYL BETAINE 
SODIUM CHLORIDE 
COCAMIDOPROPYL HYDROXYSULTAINE 
GLYCERIN 
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) 
DMDM HYDANTOIN 
EDETATE SODIUM 
CITRIC ACID MONOHYDRATE 
FD&C YELLOW NO. 5 
FD&C RED NO. 4 
Packaging
#Item CodePackage Description
1NDC:55910-294-401180 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.

← See all DG BODY ANTIBACTERIAL brands

Further information

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

Hide