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Zep Hand Sanitizer

Medically reviewed by Drugs.com. Last updated on Mar 23, 2020.

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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-462
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN 
WATER 
Packaging
#Item CodePackage Description
1NDC:66949-462-1011400 mL in 1 CASE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/23/2020
ZEP ALCOHOL SANITIZER 
ethanol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-900
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN 
WATER 
Packaging
#Item CodePackage Description
1NDC:66949-900-066000 mL in 1 CASE
2NDC:66949-900-2415140 mL in 1 CASE
3NDC:66949-900-85208198 mL in 1 BOTTLE, PLASTIC
4NDC:66949-900-891040988 mL in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/07/2000
ZEP ALCOHOL SANITIZER 
ethanol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-357
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
Packaging
#Item CodePackage Description
1NDC:66949-357-164800 mL in 1 CASE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/07/2000
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIOperations
Zep Inc.112125310manufacture(66949-357, 66949-900, 66949-462)

 
Zep Inc.

Further information

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