Zep Hand Sanitizer

Dosage form: liquid
Ingredients: ALCOHOL 62mL in 100mL
Labeler: Zep Inc.
NDC code: 66949-462

Medically reviewed by Drugs.com. Last updated on Mar 13, 2025.

66949-357/900 Alcohol Sanitizer

Active ingredient

Ethanol 62%

Purpose

Antiseptic

Uses

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

Warnings

For external use only. Do not use in the eyes, rinse promptly and thoroughly with water.

Flammable. Keep away from fire, flame or spark.

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

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

If swallowed, get medical help or contact a Poison Control Center 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.

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, Glycerin

Questions or comments?

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

ZEP HAND SANITIZER
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66949-462
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	62 mL in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN
WATER

Packaging
#	Item Code	Package Description
1	NDC:66949-462-10	11400 mL in 1 CASE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020

ZEP ALCOHOL SANITIZER
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66949-900
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	62 mL in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN
WATER

Packaging
#	Item Code	Package Description
1	NDC:66949-900-06	6000 mL in 1 CASE
2	NDC:66949-900-24	15140 mL in 1 CASE
3	NDC:66949-900-85	208198 mL in 1 BOTTLE, PLASTIC
4	NDC:66949-900-89	1040988 mL in 1 CONTAINER

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

ZEP ALCOHOL SANITIZER
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66949-357
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	62 mL in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
GLYCERIN

Packaging
#	Item Code	Package Description
1	NDC:66949-357-16	4800 mL in 1 CASE

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	Operations
Zep Inc.		112125310	manufacture(66949-357, 66949-900, 66949-462)

Revised: 03/2020

Document Id: a185a593-1fd5-908a-e053-2995a90a0c26

Set id: 021e6ca0-78fe-439c-b72b-e1d433227f0d

Version: 10

Effective Time: 20200323

Zep Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

Zep Hand Sanitizer

Further information

See also:

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Zepbound

Ozempic

Wegovy

Victoza

Saxenda

Alli

Methamphetamine

Amphetamine

Phentermine