SAFE GOOD HAND GEL- ethyl alcohol gel

Safe Good Hand Gel by

Drug Labeling and Warnings

Safe Good Hand Gel by is a Otc medication manufactured, distributed, or labeled by Jemian USA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients:

Ethyl Alcohol 62%

PURPOSE

Antiseptic

Warnings

For external use only : hands

Flammable.: keep away from fire or flame.

When Using This Product

Keep out of eyes, In case of contact with eyes, rinse with water

When Using This Product

Keep out of eyes, In case of contact with eyes, rinse with water

Stop using this product

irritation and redness develops and persists.

Keep out of reach of children.

If swallowed, get medical help promptly and Poison Control

INDICATIONS & USAGE

Kills 99% of germs!

Direction

Wet hands throughly with product and allow to dry without wiping

Other Information

do not store above 105 F

may discolor some fabric

Inactive Ingedients

water, carbomer, butylene glycol, glycerin, fragnance, triethanolamine, sodium hyaluronate

PRINCIPAL DISPLAY PANEL [image of bottle label]

INGREDIENTS AND APPEARANCE

SAFE GOOD HAND GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73917-0156
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)
ORANGE OIL (UNII: AKN3KSD11B)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TROLAMINE (UNII: 9O3K93S3TK)

Product Characteristics
Color	white	Score	no score
Shape		Size	5mm
Flavor	ORANGE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73917-0156-1	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/25/2020
2	NDC: 73917-0156-2	100 mL in 1 TUBE; Type 0: Not a Combination Product	03/25/2020
3	NDC: 73917-0156-3	30 mL in 1 POUCH; Type 0: Not a Combination Product	03/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/25/2020	12/31/2021

Labeler - Jemian USA Inc. (078822273)