HAND SANITIZER GEL- ethyl alcohol gel

Hand Sanitizer Gel by

Drug Labeling and Warnings

Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by NV Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient Purpose

Ethyl Alcohol 70% v/v Antimicrobial

USES

• Hand Sanitizer to help reduce bacteria on the skin that could cause disease
• Recommended for repeated use

WARNING

Warnings

Flammable Keep away from Flame

For External Use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appeara and lasts

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

Directions

Directions

• Place enough product in your palm to thoroughly cover your hands
• Rub hands together briskly until dry
• Children under 6 years of age should be supervised when using this product

Other information

Other Information

• Store below 110F (43C) May discolor certain fabrics or surfaces

In active Ingredients

Water (Aqua) , Glycerin, Aloe Barbadensis Leaf Juice,, Tocopheryl Acetate, Carbomer, Triethanolamine, Fragrance (Parfum)

Manufactured By: Questions or Comments

Manufactured By: Reforma Group, Southfield, Michigan 48033

Questions or comments? Call 1-248-358-9022

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.

Purpose

Antimicrobial

PRINCIPLE DISPLAY PANEL

HAND SANITIZER GEL

MADE IN USA

NDC: 73696-100-04

KILLS 99.99% of Germs

4 fl. oz (120 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73696-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.001 mL  in 100 mL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	0.35 mL  in 100 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.25 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	34.278 mL  in 100 mL
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.001 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73696-100-04	120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/31/2020

Labeler - NV Labs (019662814)

Registrant - NV Labs (019662814)

Establishment
Name	Address	ID/FEI	Business Operations
NV Labs		019662814	manufacture(73696-100)