Defense Zone Hand Sanitizer

Defense Zone by

Drug Labeling and Warnings

Defense Zone by is a Otc medication manufactured, distributed, or labeled by Prime Enterprises. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DEFENSE ZONE HAND SANITIZER- ethyl alcohol gel 
Prime Enterprises

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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Defense Zone Hand Sanitizer

Active Ingredient(s)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

For external use only. Flammable. Keep away from heat or flame

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin. do not inhale or ingest.

Stop use and ask a doctor if irritation and redness develops. condition persists more than 72 hours.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • wet hands thoroughly with product and allow to dry without wiping.
  • for children under 6, use only under adult supervision not recommended for infants.

Other information

  • do not store above 104 F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

Aloe Barbadensis Leaf juice, Aminomethyl Propanol, Carbomer, Isopropyl Myristate, Glycerin, Tocopherol, water

Defense zone Hand Sanitizer

Principal Display Label

DEFENSE ZONE  HAND SANITIZER
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 58443-0344
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
TOCOPHEROL (UNII: R0ZB2556P8)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
CARBOMER 934 (UNII: Z135WT9208)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
Product Characteristics
Colorwhite (clear) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 58443-0344-5354 mL in 1 BOTTLE; Type 0: Not a Combination Product03/13/202006/30/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/13/202006/30/2022
Labeler - Prime Enterprises (101946028)
Registrant - Prime Enterprises (101946028)
Establishment
NameAddressID/FEIBusiness Operations
Prime Enterprises101946028manufacture(58443-0344) , analysis(58443-0344) , label(58443-0344) , pack(58443-0344)

Revised: 4/2022
 

Trademark Results [Defense Zone]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DEFENSE ZONE
DEFENSE ZONE
86903251 5229002 Live/Registered
Australian Gold, LLC
2016-02-10
DEFENSE ZONE
DEFENSE ZONE
77611002 3729725 Dead/Cancelled
Australian Gold, Inc.
2008-11-10

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