Active Ingredient
Isopropyl Alcohol 75% v/v
Prevent Foam Sanitizer
FDA Label NDC 78835-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Eco-med Pharmaceuticals, Inc. for the product Prevent Foam Sanitizer (NDC 78835-002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings., keep out of reach of children., directions, inactive ingredients:, for domestic/personal care use., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
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: [email protected]
Package Labeling:
Bottle (Bottle)
Package Labeling:78835-002-37
Label6 (Label6)
* Please review the disclaimer below.
