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 SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD. 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 and other microbes

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

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 right away.

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 104° F
■ may discolor some fabrics ■ harmful to some wood
finishes.

Inactive ingredients

Water,Peg-40 hydrogenated, Castor oil, Carbomer,Sodium hydroxide, aloe vera extract

DESCRIPTION

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

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

SUPPRESS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74913-610
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.05 mL  in 100 mL
SODIUM HYDROXIDE (UNII: 55X04QC32I)	0.12 mL  in 100 mL
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)	0.5 mL  in 100 mL
CARBOMER 940 (UNII: 4Q93RCW27E)	0.3 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	24.03 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74913-610-01	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD (546345856)

Registrant - SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD (546345856)

Establishment
Name	Address	ID/FEI	Business Operations
SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD		546345856	manufacture(74913-610)