BEN E.KEITH HAND CLEANER- ethyl alcohol gel

Ben E.Keith by

Drug Labeling and Warnings

Ben E.Keith by is a Otc medication manufactured, distributed, or labeled by Ben E. Keith. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62% v/v

Purpose

Antibacterial Agent

Uses

For handwashing to decrease bacteria on skin.

Warnings

For external use only

Flammable Keep away from heat or flame.

Do not use in Eyes

Stop use if redness and irritation develop.  If condition persists for more than 72 hours, consult a physician.

Stop use if redness and irritation develop. If condition persists for more than 72 hours, consult a physician.

Keep out of reach of children.  If swallowed, contact a physician or poison control center.

Directions

To decrease bacterial on skin, apply a small amount to palm.  Briskly rub, covering hands withproduct until dry.

Inactive ingredients

Water, glycerin, propylene glycol, isopropyl myristate, aloe barbadensis leaf, tocopheryl acetate (Vitamin E), Carbomer, Aminomethyl propanol.

Principal Display Panel and representative label

DELIVERING QUALITY SINCE 1906

BEN E. 

KEITH

CO.

FOODSERVICE DISTRIBUTORS

GEL INSTANT HAND SANITIZER

Net Contents: 8 Fl. Oz. (237 mL)

Distributed by:

BEN E. KEITH FOODS Fort Worth, TX 76101

MADE IN USA

INGREDIENTS AND APPEARANCE

BEN E.KEITH  HAND CLEANER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50980-056
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER 1342 (UNII: 809Y72KV36)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50980-056-19	237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/02/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/02/2009

Labeler - Ben E. Keith (007929748)