HAND SANITIZER- alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Tecnoglobal Ph7, S.a. De C.v., Tecnoglobal Ph7 S.a De C.v.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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 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

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water, PEG-12 Dimethicone, Glycerin, Carbomer, Propylene Glycol, Aminomethyl Propanol, Phenoxyethanol, Iodoprpynyl Butylcarbamate, Tetrasodium EDTA, Ext. Violet 2, Aloe Barbadensis Leaf Juice

Package Label - Principal Display Panel

30mL NDC: 75470-110-05

60mL NDC: 75470-110-04

900mL NDC: 75470-110-03

400mL NDC: 75470-110-02

251mL NDC: 75470-110-01

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75470-110
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
CARBOMER 940 (UNII: 4Q93RCW27E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75470-110-01	251 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 75470-110-02	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 75470-110-03	900 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 75470-110-04	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC: 75470-110-05	30 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 - Tecnoglobal Ph7, S.a. De C.v. (813006665)

Establishment
Name	Address	ID/FEI	Business Operations
Tecnoglobal Ph7 S.a De C.v.		813006665	manufacture(75470-110)