PREVENT SANITIZER- isopropyl alcohol gel 
Eco-Med Pharmaceuticals, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Prevent+ Gel Sanitizer

Drug Facts

Active ingredient

Isopropyl Alcohol 75% v/v

Purpose

Antimicrobial

Uses

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

Label

Package Labeling:78835-001-16

Label3

Package Labeling:78835-001-08

Label4

Package Labeling:78835-001-37

Label5

PREVENT SANITIZER 
isopropyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78835-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78835-001-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2020
2NDC:78835-001-16500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2020
3NDC:78835-001-08250 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2020
4NDC:78835-001-373785 mL in 1 JUG; Type 0: Not a Combination Product08/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/30/2020
Labeler - Eco-Med Pharmaceuticals, Inc. (249183435)
Establishment
NameAddressID/FEIBusiness Operations
Eco-Med Pharmaceuticals, Inc.249183435manufacture(78835-001) , label(78835-001) , pack(78835-001)

Revised: 8/2020
Document Id: ac8b722a-8483-2b23-e053-2a95a90a56eb
Set id: ab97b13c-6114-25a4-e053-2995a90a90be
Version: 2
Effective Time: 20200810
 
Eco-Med Pharmaceuticals, Inc.