HILL COUNTRY ESSENTIALS ANTIBACTERIAL- triclosan soap

Hill Country Essentials by

Drug Labeling and Warnings

Hill Country Essentials by is a Otc medication manufactured, distributed, or labeled by HEB. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

hce7.5.jpg

INGREDIENTS AND APPEARANCE

HILL COUNTRY ESSENTIALS  ANTIBACTERIAL
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-220
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.15 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-220-08	222 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/07/2010

Labeler - HEB (007924756)