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Zep Alcohol Sanitizer

Dosage form: liquid
Ingredients: ALCOHOL 6.2mL in 10mL
Labeler: Zep Inc.
NDC Code: 66949-900

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Zep Alcohol Sanitizer

Active ingredient

Alcohol 62%

Purpose

Antiseptic

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

Warnings

For external use only.

Flammable. Keep away from fire, flame or spark.

When using this product

  • Avoid eye contact.
  • If in eyes, rinse promptly and thoroughly with water.

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

Water, Glycerine

Questions or comments?

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

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) ALCOHOL6.2 mL  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
Packaging
#Item CodePackage Description
1NDC:66949-900-001000 mL in 1 BOTTLE, PLASTIC
2NDC:66949-900-213785 mL in 1 BOTTLE, PLASTIC
3NDC:66949-900-85208198 mL in 1 BOTTLE, PLASTIC
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) ALCOHOL6.2 mL  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
Packaging
#Item CodePackage Description
1NDC:66949-357-151200 mL in 1 BOTTLE, PLASTIC
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.030471374manufacture(66949-900, 66949-357)

Revised: 11/2016
 
Zep Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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