HAND SANITIZER- alcohol gel

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by EXPORTADORA IN & OUT S DE RL DE CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ethyl alcohol v/v - 70%

Purposes

Antimicrobial

Uses

hand sanitizer to decrease bacteria on the skin that could cause disease

recommended for repetead use

warnings

for external use only: hands

flammable, keep away from fire and flame

When using this product

keep out of eyes, do not use in or near the eyes

in case of contact with eyes, flush thorougly with water

avoid contact with broken skin

do not inhale or ingest

When using this product

keep out of eyes, do not use in or near the eyes

in case of contact with eyes, flush thorougly with water

avoid contact with broken skin

stop use and ask a doctor if

irritation and redness develo

condition persists for more than 72 hours

Keep out of reach of children

if swallowed, get medical help or contact a posion control center right away

Directions

put enough product in your palm to cover hands and rub hands together briskly until dry without wiping

for children under 6 years of age should be supervised when using ozone

not recommended for infants

Other information

store below 105 F (40C)

may discolor certain fabrics

harmful to wood finishes and plastics

Inactive ingredients

Purified water (aqua), Vegetable Glycerin, Carboxymethyl cellulose, Hydroxypropyl methylcellulose hpmc, orange oil

Question or comments

visit www.jsglobal.biz

Principal Display

Efficiently kills 99.9%

of most illness causing germs

leaves hands soft

contain moisturizers

paraben free

phtalate free

formaldehyde donor free

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77210-0012
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
GLYCERIN (UNII: PDC6A3C0OX)
ORANGE OIL (UNII: AKN3KSD11B)
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
HYPROMELLOSE 2208 (60000 MPA.S) (UNII: 2F7T07H9ZD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77210-0012-1	3800 mL in 1 JUG; Type 0: Not a Combination Product	06/26/2020
2	NDC: 77210-0012-2	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/26/2020
3	NDC: 77210-0012-3	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/26/2020
4	NDC: 77210-0012-4	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/26/2020

Labeler - EXPORTADORA IN & OUT S DE RL DE CV (951577298)