HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by GoodFibers, Biotechnologia Educacion y Genetica, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

Uses

• Hand sanitizer to decrease bacteria on the skin
• Recommended for repeated use

Warnings

Warnings

For external use only Flammable

• Keep away from fire or flame

When using

When using this product:

• Do not use in or near eyes

If contact occurs, rinse eyes thoroughly with water.

Stop use

Stop use and ask a doctor

• If irritation and redness persist for more than 72 hours.

Keep out of reach

Keep out of reach of children

In case of accidental ingestion, seek medical attention or contact a poison control centerimmediately

Directions

Directions

• Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry.
• Children under six years of age should be supervised when using this product.

Other information

Other Information

• Store at 1 oC - 30 oC (34 oF - 86 oF)

Inactive ingredients

Inactive Ingredients

Carbomer, Glycerin, Triethanolamine, Water

PDP

Ethyl Alcohol

70%

all clear

Hand

Sanitizer

Fragrance Free

Kills 99.99 of germs

16.9 fl oz 500ml

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77070-700
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
ACRYLIC ACID (UNII: J94PBK7X8S)

Product Characteristics
Color	white (Clear colorless)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77070-700-80	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/07/2020

Labeler - GoodFibers (105870470)

Registrant - GoodFibers (105870470)