HILL COUNTRY ESSENTIALS ANTIBACTERIAL- triclosan soap 
HEB

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.

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Active Ingredient

Triclosan 0.15%

Purpose

Antibacterial

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 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 refile for a dispensing bottle. From dispensing bottle, apply onto wet hands and work into a lather, rinse thoroughly.

Uses

To help reduce bacteria on the skin

Inactive Ingredients

Water (Aqua), Sodium Laureth Sulfate, Ammonium Lauryl Sulfate, Decyl Glucoside, Cocamidopropyl Betaine, Glycerin, Sodium Chloride, PEG-18 Glyceryl Oleate/cocoate, Fragrance (Parfum), Cocamide MEA, DMDM Hydantoin, Tetrasodium EDTA, Citric Acid,Yellow 5 (CI 19140), Red 4 (CI 14700)

Package Front and Back Labels

hce64.jpg64 OZ Front and Back Labels

HILL COUNTRY ESSENTIALS  ANTIBACTERIAL
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-220
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.15 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
EDETATE SODIUM (UNII: MP1J8420LU)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-220-641892 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/07/2010
Labeler - HEB (007924756)

Revised: 10/2010
Document Id: 9ad63cc4-b300-4634-a34d-b1fab1aa30d8
Set id: b722ad2f-29f3-4abb-b2de-2fcef7be6be6
Version: 1
Effective Time: 20101007
 
HEB