GERM FREE HAND SANITIZER TRAVEL PACK- alcohol spray 
Tallon Enterprises LLC

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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Germ Free Hand Sanitizing Spray Travel Pack

Active Ingredient(s)

Ethyl Alcohol 80% v/v.

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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.

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

Other information

Inactive ingredients

aloe vera, glycerin, hydrogen peroxide, peppermint & eucalyptus essential oil, vitamin E

Package Label - Principal Display Panel

59.15 mL NDC: 80150-530-97

Front Label

Back Label

GERM FREE HAND SANITIZER TRAVEL PACK 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80150-530
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL  in 100 mL
EUCALYPTUS OIL (UNII: 2R04ONI662)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80150-530-9759.15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/14/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/14/2020
Labeler - Tallon Enterprises LLC (117624756)

Revised: 12/2020
Document Id: b66f890a-a154-2b00-e053-2995a90a9a8e
Set id: b67010e3-55fc-3093-e053-2a95a90aaec7
Version: 1
Effective Time: 20201214
 
Tallon Enterprises LLC