PREVENT FOAM SANITIZER- isopropyl alcohol liquid 
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.

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Prevent+ Foam 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, Cocamidopropyl betaine, Bis-PEG-12 Dimethicone, Glyceryl Caprylate, Dimethyl Lauramide, 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:

Bottle

Package Labeling:78835-002-37

Label6

PREVENT FOAM SANITIZER 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78835-002
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)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
N,N-DIMETHYLLAURAMIDE (UNII: 04BJ5OT1PA)  
BIS-PEG-12 DIMETHICONE (70 MPA.S) (UNII: 2JDK5W22H4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78835-002-16500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2020
2NDC:78835-002-373785 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)

Revised: 8/2020
Document Id: ac8b9268-a058-4033-e053-2995a90a5655
Set id: ac2348e1-4937-3f92-e053-2995a90a0d73
Version: 2
Effective Time: 20200810
 
Eco-Med Pharmaceuticals, Inc.