INSTAFRESH- alcohol liquid

InstaFresh by

Drug Labeling and Warnings

InstaFresh by is a Otc medication manufactured, distributed, or labeled by DSHealthcare, Central Solutions Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Ethyl Alcohol 70% (v/v)

PURPOSE

Purpose

Hand Sanitizer

INDICATIONS & USAGE

Uses

Helps reduce potentially harmful pathogens from hands

Helps prevent cross contamination by hand contact

Helps prevent drying and chafing of skin

Recommended for repeated use

WARNINGS

Warnings

For External use only

Flammable, keep away from fire or flame

When using this product

Do not use in or near the eyes

Avoid contact with broken skin

Use in well-ventilated area

Discontinue use if irritation and/or redness develops

Keep out of reach of children.

In case of accidental ingestion, seek medical attention or contact Poison Control Center immediately

DOSAGE & ADMINISTRATION

Directions

Wet hands thoroughly with product, covering entire surface of hands, including fingertips, cuticles, wrists and forearms

Rub vigorously into skin until dry

No rinsing or toweling required

STORAGE AND HANDLING

Other Information

Store in a cool dry place below 104 F

INACTIVE INGREDIENT

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, EDTA, Glycerin. Tetrahydroxypropyl Ethylenediamine and Water

QUESTIONS

Questions or Comments

For product or technical information contact Sultan Chemists Inc. at 201-871-1232, toll free 1-800-637-8582 or visit our website at www.sultanchemists.com

PRINCIPAL DISPLAY PANEL

InstaFresh

Instant Hand Sanitizer

70% Ethanol Formulation provides effective decontamination

Moisturizers leave hands feeling soft and clean

Dries quickly without sticky residue

Low viscosity allows for easier, faster coverage

Complies with CDC Hand Hygiene Recommendations

Ideal for use in the Touch Less Sanitizer Dispenser

REF 95708

CONTENTS: 1 Gallon (3.8L)

INGREDIENTS AND APPEARANCE

INSTAFRESH 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-0957
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)) (UNII: 59TL3WG5CO)
EDETIC ACID (UNII: 9G34HU7RV0)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
EDETOL (UNII: Q4R969U9FR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0699-0957-04	118 mL in 1 BOTTLE, PLASTIC
2	NDC: 0699-0957-08	532 mL in 1 BOTTLE, PLASTIC
3	NDC: 0699-0957-02	946 mL in 1 BOTTLE, PLASTIC
4	NDC: 0699-0957-01	3785 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/2005

Labeler - DSHealthcare (056296981)

Establishment
Name	Address	ID/FEI	Business Operations
Central Solutions Inc		007118524	manufacture