ZEP ALCOHOL SANITIZER- ethanol liquid

Zep Alcohol Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethanol 66%

Uses

• Hand sanitizing to decrease bacteria on skin.
• No rinsing required.

Warnings

For external use only.
Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.
Flammable. Keep away from fire, flame or spark.

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 a 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.

ASK DOCTOR

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

Directions

• Wet hands thoroughly with spray mist.
• 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.

INDICATIONS & USAGE

• Wet hands thoroughly with spray mist.
• 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

Store at 20 to 25°C (68 to 77°F).

Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Deionized water; Glycerine

Questions or comments?

Call 1-877-I-BUY-ZEP (1-877-428-9937)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP ALCOHOL SANITIZER 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	66 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-102-01	11400 mL in 1 CASE; Type 0: Not a Combination Product	08/07/2000
2	NDC: 66949-102-06	6000 mL in 1 CASE; Type 0: Not a Combination Product	08/07/2000
3	NDC: 66949-102-24	15140 mL in 1 CASE; Type 0: Not a Combination Product	08/07/2000
4	NDC: 66949-102-85	208198 mL in 1 DRUM; Type 0: Not a Combination Product	08/07/2000
5	NDC: 66949-102-89	1040988 mL in 1 CONTAINER; Type 0: Not a Combination Product	08/07/2000

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/07/2000

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-102)