SUPPRESS HAND SANITIZER- alcohol gel

SUPPRESS Hand Sanitizer by

Drug Labeling and Warnings

SUPPRESS Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by HD Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

to decrease bacteria on the skin.

Warnings

For external use only. Do not inhale or ingest. Flammable. Keep away from heat or flame when using this product.

Do not use

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

WHEN USING

When using this product keep away from eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

STOP USE

Stop use and ask a physician if skin irritation occurs.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Apply to hands thoroughly and rub vigorously until dry.
• For children under 6 years, use only with adult supervision.
• Not recommended for infants.

Other information

• Do not store above 104F (40C)
• May discolor some fabrics
• harmful to some wood finishes

Inactive ingredients

purified water USP

PEG-40 hydrogenated castor oil

carbomer

sodium hydroxide

aloe vera extract

Package Label - Principal Display Panel

500 mL NDC: 77343-111-01

Distributed By:

Distributed by: HD Group LLC 335 N Edgewood Ln, Suite 130 Eagle, ID 83616

INGREDIENTS AND APPEARANCE

SUPPRESS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77343-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
CARBOMER 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77343-111-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - HD Group LLC (833742898)