Med X Frontline Advanced Hand Sanitizer with Moisturizers & Vitamin E

Med X Frontline Advanced Hand Sanitizer with Moisturizers and Vitamin E by

Drug Labeling and Warnings

Med X Frontline Advanced Hand Sanitizer with Moisturizers and Vitamin E by is a Otc medication manufactured, distributed, or labeled by Zhejiang iColor Biotech Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MED X FRONTLINE ADVANCED HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- alcohol gel 
Zhejiang iColor Biotech Co., Ltd

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Med X Frontline Advanced Hand Sanitizer with Moisturizers & Vitamin E

Drug Facts

Active Ingredients

Ethyl alcohol 75% v/v

Purpose

Antiseptic

Uses

• For hand washing to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are not available.

Warnings

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

When using this product

do not use in or near 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 appears on the skin.

Keep out of reach of children.

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

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Children under 6 years of age should be supervised by adult when applying this product.
• Do not use on children less than 2 months of age or on open skin wounds.

Other information

• Store between 15-30 oC (59-86°F)
• Avoid freezing and excessive heat above 40°C (104°F)
• May discolor some fabrics or surtaces

Inactive ingredients

Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose,Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyi Propanol.

Package Labeling(236 ml)

Package Labeling(3.8 L)

Package Labeling(500 ml)

MED X FRONTLINE ADVANCED HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-073
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SQUALANE (UNII: GW89575KF9)
PANTHENOL (UNII: WV9CM0O67Z)
INULIN (UNII: JOS53KRJ01)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
FRUCTOSE (UNII: 6YSS42VSEV)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-073-01	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/05/2020	01/31/2026
2	NDC: 74934-073-02	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/05/2020	01/31/2026
3	NDC: 74934-073-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/05/2020	01/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/05/2020	01/31/2026

Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)

Revised: 1/2024

Document Id: 0fb44d72-fdb1-4341-e063-6294a90ae9cf

34390-5

Set id: b5577617-e0bb-7381-e053-2a95a90a5568

Version: 2

Effective Time: 20240124