ZEP PROFESSIONAL ALCOHOL HAND SANITIZING- ethanol liquid

Zep Professional Alcohol Hand Sanitizing by

Drug Labeling and Warnings

Zep Professional Alcohol Hand Sanitizing by is a Otc medication manufactured, distributed, or labeled by Zep Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethanol 60%

Purpose

Antiseptic

Uses

• Hand sanitizing to decrease bacteria on skin.
• Recommended for repeated use.
• No rinsing required.

Warnings

For external use only.

Flammable. Keep away from fire, flame or spark.

Do not use in eyes; if in eyes, rince thoroughly with water.

WHEN USING

When using this product

• Do not swallow.
• If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

STOP USE

Stop use and ask doctor if skin irritation or redness persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

• Use pump and apply gel to hands
• Rub hands together allowing liquid to contact all areas, especially around the nails and cuticles.
• Continue rubbing vigorously until hands are dry.
• No rinsing or toweling is required.

Other information

• Keep container closed and stored in a dry area at temperatures between 40°F and 120°F.
• Do not reuse empty container.
• Dispose in accordance with all applicable federal, state & local regulations.

Inactiv ingredients

Deionized Water, Diisopropanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance

Questions or comments?

Call 1-800-I-BUY-ZEP (1-800-428-9937)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP PROFESSIONAL ALCOHOL HAND SANITIZING 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-109
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-109-01	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2009
2	NDC: 66949-109-24	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2009

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-109)