Zepaseptic by Zep Inc. Zepaseptic

Zepaseptic by

Drug Labeling and Warnings

Zepaseptic by is a Otc medication manufactured, distributed, or labeled by Zep Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ZEPASEPTIC- chloroxylenol 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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Zepaseptic

Active ingredient

Chloroxylenol 0.2%

Purpose

Antiseptic Hand Wash

Uses

Hand sanitizing to decrease bacteria on the skin.

Warnings

For external use only.

When using this product

  • Keep out of eyes.
  • If in eyes, rinse promptly and thoroughly with water.

Stop use and ask a 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 with water.
  • Apply liquid soap.
  • Massage soap into hands and wrists, emphasizing the back of hands, knuckles and cuticles.
  • Rinse hands thoroughly and dry.

Other information

  • Store at 20 to 25°C (68 to 77°F).
  • Dispose in accordance with all applicable federal, local and state regulations.

Inactive ingredients

Water, Oleamide MEA, Lauramide MEA, Propylene Glycol, Cocamide DIPA, Tetrasodium EDTA, Alcohol, Triclosan, Fragrance, Acrylates/PEG-10 Maleate/Styrene Copolymer, BHT, Yellow 5, Green 3

Questions or comments?

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

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ZEPASEPTIC 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66949-928
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
OLEIC ACID (UNII: 2UMI9U37CP)  
LAURIC ACID (UNII: 1160N9NU9U)  
MONOETHANOLAMINE (UNII: 5KV86114PT)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
ALCOHOL (UNII: 3K9958V90M)  
TRICLOSAN (UNII: 4NM5039Y5X)  
METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Product Characteristics
ColorgreenScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 66949-928-213785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/20/198901/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/20/198901/01/2020
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.030471374manufacture(66949-928)

Revised: 12/2017
 
Zep Inc.