ALCOHOL FOAM SAN- alcohol liquid 
Zep Inc.

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.

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Alcohol Foam San

Active ingredient

Ethanol 62%

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.

Avoid contact with eyes. Can cause eye irritation.

When using this product

  • do not use in or around eyes. If eye contact occurs, rinse well with water for at least 15 minutes. Consult a physician.
  • do not swallow this product. If swallowed, do not induce vomiting. If individual is conscious, give large quantites of water to drink and consult a physician immediately.

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children and pets.

Directions

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • No rinsing or toweling is required

Other information

  • May discolor certain fabrics or surfaces.
  • Keep container closed.
  • Store at temperatures between 40F and 120F.
  • Do not reuse empty container.
  • Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

deionized water, diethanolamine bis(C8-C18 perfluoroalkylethyl)phosphate, glycerin, fragrance

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ALCOHOL FOAM SAN 
ethanol liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:66949-014
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 
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE 
GLYCERIN 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-014-00550 mL in 1 BOTTLE, PLASTIC
2NDC:66949-014-011000 mL in 1 BOTTLE, PLASTIC
3NDC:66949-014-243785 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/07/200808/16/2013
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.030471374manufacture(66949-014)

Revised: 12/2013
 
Zep Inc.