ZEP INSTANT HAND SANITIZER- 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 Sanitizer Gel

Active Ingredient

Alcohol 60%

Purpose

Antiseptic

Uses

Warnings

For external use only.

Flammable. Keep away from fire, flame or spark.

​When using this product

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

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

Keep out of reach of children and pets.

Directions

Other information

Inactive ingredients

Deionized Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Diisopropanolamine, Fragrance

Questions or comments?

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

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ZEP INSTANT HAND SANITIZER 
ethanol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-878
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 6 mL  in 10 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66949-878-00 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2 NDC:66949-878-05 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3 NDC:66949-878-21 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/29/2004
ZEP INSTANT HAND SANITIZER 
ethanol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-246
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 6 mL  in 10 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66949-246-15 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/29/2004
ZEP INSTANT HAND SANITIZER 
ethanol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-908
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 6 mL  in 10 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66949-908-01 118.3 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/29/2004
Labeler - Zep Inc. (030471374)
Establishment
Name Address ID/FEI Business Operations
Zep Inc. 030471374 manufacture(66949-878, 66949-246, 66949-908)

Revised: 12/2015
Document Id: 2691a067-431c-0deb-e054-00144ff88e88
Set id: bd7e3d4f-b397-4f39-9692-1a13f232eb71
Version: 4
Effective Time: 20151210
 
Zep Inc.