PREVENT SANITIZER- isopropyl alcohol gel

Prevent Sanitizer by

Drug Labeling and Warnings

Prevent Sanitizer by is a Otc medication manufactured, distributed, or labeled by Eco-Med Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl Alcohol 75% v/v

Purpose

Antimicrobial

Uses

• For personal hand hygiene to help prevent the spread of bacteria. For occasional use.

Warnings.

Flammable. Keep away from open flame and sources of heat

Keep out of reach of children.

Supervise children when they use this product.

For external use only. If accidental ingestion occurs, call a Poison Control Center immediately.

Avoid contact with the eyes. If contact occurs, flush eyes with water. If irritation develops, discontinue use and consult a health care practitioner.

Directions

- Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive Ingredients:

Water, Carbomer, Triethanolamine, Glycerin, Aloe Barbadensis Leaf Powder, DL-alpha Tocopheryl Acetate (Vitamin E)

For domestic/personal care use.

Store below 43° C (110° F).

May discolour certain fabrics.

Questions :

1-844-432-6633 Mon -Fri 8am - 4pm (EST)

Email: info@eco-med.com

Package Labeling:78835-001-02

Package Labeling:78835-001-16

Package Labeling:78835-001-08

Package Labeling:78835-001-37

INGREDIENTS AND APPEARANCE

PREVENT SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78835-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78835-001-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2020
2	NDC: 78835-001-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2020
3	NDC: 78835-001-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2020
4	NDC: 78835-001-37	3785 mL in 1 JUG; Type 0: Not a Combination Product	08/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/30/2020

Labeler - Eco-Med Pharmaceuticals, Inc. (249183435)

Establishment
Name	Address	ID/FEI	Business Operations
Eco-Med Pharmaceuticals, Inc.		249183435	manufacture(78835-001) , label(78835-001) , pack(78835-001)