ECOPURE HAND SANITIZER- alcohol gel

ECOPURE HAND SANITIZER by

Drug Labeling and Warnings

ECOPURE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Adrian Rivera Maynez Enterprises Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

to help reduce germs and bacteria on the skin

Warnings

For external use only

• Flammable
• Keep away from sources of fire or heat
• Do not ingest

When using this product

avoid contact with eyes. If contact with eyes occurs, rinse thoroughly with clean water.

STOP AND CONSULT YOUR DOCTOR

If irritation or redness occurs

Keep out of Reach of Children.

In case of accidental ingestion contact the your local or national poison control center immediately 1-800-222-1222

Directions

• Wet hands thoroughly with product and rub together vigorously until dry.

Other information

Store at a temperature below 106° degrees F (41° C)

Questions or comments:

888-735-3621

Inactive ingredients:

D-Water, Aloe Vera (Leaf), Isopropyl Alcohol, Glycerin, Propylene Glycol, hydrogen Peroxide, Carbomer, Triethanolamine, Fragrance, FD&C Blue #1 and Yellow #5

Package Labeling:

INGREDIENTS AND APPEARANCE

ECOPURE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79241-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79241-000-00	429 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/01/2020

Labeler - Adrian Rivera Maynez Enterprises Inc (013690640)