HUMAN GUARD SANITIZER- alcohol aerosol, spray

Human Guard Sanitizer by

Drug Labeling and Warnings

Human Guard Sanitizer by is a Otc medication manufactured, distributed, or labeled by DERMACOS KOREA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antimicrobial

Purpose

Antimicrobial, Hand Sanitizer

Use

To help reduce bacteria on the skin.

Warnings

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

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

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

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

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

Directions

• Open package and apply wipe throughly to hands.
• Allow to dry without wiping.
• Children under 6 years of age should be supervised when using this product.
• Not recommended for infants.

Other information

• Store at room temperature (33.8oF-86oF, 1oC-30oC) and avoid cold or dry place.
• May discolor certain fabrics or surfaces.
• Harmful to wood finishes and plastics.

Inactive ingredients

Fragrance (Lemon), Glycerin, Purified Water, Sodium Hyaluronate.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HUMAN GUARD SANITIZER 
alcohol aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77637-500
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77637-500-01	17 mL in 1 BOX, UNIT-DOSE; Type 0: Not a Combination Product	04/29/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/29/2021

Labeler - DERMACOS KOREA (695625857)

Registrant - DERMACOS KOREA (695625857)

Establishment
Name	Address	ID/FEI	Business Operations
DERMACOS KOREA		695625857	manufacture(77637-500)