Travel Lite Hand Sanitizing Gel

Travel Lite Hand Sanitizing Gel by

Drug Labeling and Warnings

Travel Lite Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by Diamond Wipes International, Inc, Diamond Wipes International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TRAVEL LITE HAND SANITIZING GEL- travel lite hand sanitizing gel gel 
Diamond Wipes International, Inc

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Travel Lite Hand Sanitizing Gel

Active Ingredient(s)

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

for hand sanitizing to decrease bacteria on skin

recommended for repeated use

Warnings

• For external use only
• Flammable, Keep away from heat or flame

When using this product

avoid contact with eyes. if in eyes, flush with water

do not ingest

Discontinue use and contact a doctor

if irritation and redness develop and conditions persist for more than 72 hours

Keep out of reach of children.

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

Directions

place small amount in your palm and rub hands together until dry

children under 6 years of age should be supervised when using this product

Other information

do not store above 110F (43C)

store in an area inaccessible to children

Inactive ingredients

Water, Glycerin, Chamomilla Recutita (Matricaria) Flower Extract, Cucumis Sativus (Cucumber) Fruit Extract, Althaea Officinalis Root Extract, Avena Sativa (Oat) Kernel Extract, Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Fragrance

Label

travel lite TM

MAKE IN U.S.A. with global components

HAND SANITIZING WIPES

kills 99.9% of germs

Alcohol-based

Moisturizing formula with aloe

and botanical extracts

Vegan Cruelty-Free Gluten-Free Non-Gmo

Sulfate-Free Phthalate-Free Triclosan-Free

Net Wt. 0.04Fl OZ / 1.2mL

©2020 Diamond Wipes International, Inc. All rights reserved.

Chino, CA91710 Wipes123.com

800-454-1077

TRAVEL LITE HAND SANITIZING GEL 
travel lite hand sanitizing gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64709-177
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
OAT (UNII: Z6J799EAJK)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CHAMOMILE (UNII: FGL3685T2X)
CUCUMBER (UNII: YY7C30VXJT)
ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64709-177-10	1 mL in 1 PACKET; Type 0: Not a Combination Product	10/19/2020	12/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/19/2020	12/31/2023

Labeler - Diamond Wipes International, Inc (161104729)

Registrant - Diamond Wipes International, Inc (161104729)

Establishment
Name	Address	ID/FEI	Business Operations
Diamond Wipes International, Inc.		161104729	manufacture(64709-177)

Revised: 5/2026

Document Id: 51522434-0869-5220-e063-6294a90ae9c5

34390-5

Set id: b6acf189-2978-41c3-e053-2a95a90ac933

Version: 5

Effective Time: 20260508