HAND SANITIZER- alcohol gel

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by MARGREY INDUSTRIAL SA DE CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol v/v 60-80%

Purposes

Antimicrobial

Uses

Hand sanitizer to decrease virus and 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

Do not inhale or ingest

Stop use and ask a doctor if

irritation and redness develop

condition persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away

keep out of reach of children

if swallowed, get medical help or contact a poison 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 this product

not recommended for infants

other information

store below 105 f 40 c

may discolor certain fabrics

harmful to wood finishes and plastics

inactive ingredients

purified water, hydroxypropyl methylcellulose hpmc, carboxymethyl cellulose, carbomer, glycerine usp

questions or comments

visit www.cleanspure.com

PRINCIPAL DISPLAY

ADVANCED HAND SANITIZER

KEEP HANDS FEELING SOFT

TRUSTED FORMULA

MAZIMUN PROTECTION

REFRESHING GEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74543-193
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
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)	0.1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	29.6 mL  in 100 mL
HYPROMELLOSE 2208 (60000 MPA.S) (UNII: 2F7T07H9ZD)	0.1 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.2 mL  in 100 mL
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)	0.4 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74543-193-12	1000 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	06/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/11/2020

Labeler - MARGREY INDUSTRIAL SA DE CV (814572392)

Registrant - MARGREY INDUSTRIAL SA DE CV (814572392)

Establishment
Name	Address	ID/FEI	Business Operations
MARGREY INDUSTRIAL SA DE CV		814572392	manufacture(74543-193) , pack(74543-193) , label(74543-193)