SOFT CARE FRAGRANCE FREE INSTANT HAND SANITIZER- alcohol liquid

Soft Care Fragrance Free Instant Hand Sanitizer by

Drug Labeling and Warnings

Soft Care Fragrance Free Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Diversey, Inc., Kutol Products Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Ethyl alcohol 62%

PURPOSE

Purpose

Skin Antiseptic

INDICATIONS & USAGE

Uses

To decrease bacteria on hands.

WARNINGS

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product

Do not use in the eyes.

In case of contact, immediately flush with water.

Stop use and ask a doctor if

irritation and redness develop.

If condition persists for more than 72 hours, consult a doctor.

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

Apply 1-2 ml into hands, rub product vigorously over hands covering all surfaces.

Allow to air dry.

REFERENCES

Other information

EMERGENCY PHONE: 1-800-851-7145

See MSDS MS0301331

Store below 35 C (95 F)

See container for lot number and expiration date.

Do not contaminate water, food or feed during use, storage or disposal.

FOR COMMERCIAL and INDUSTRIAL USE ONLY

INACTIVE INGREDIENT

Inactive ingredients

Water, Glycerin, Carbomer, Proplene glycol, Isopropyl myristate, Aminomethyl propanol, Aloe Barbadensis Leaf Juice, Tocopheryl acetate

QUESTIONS

Questions or comments?

1-800-558-2332 Monday through Friday 7:30 AM to 5:00 PM Central Standard Time

www.diversey.com

PRINCIPAL DISPLAY PANEL

Sealed Air

Diversey Care

Diversey

Soft Care

Fragrance Free

Instant Hand Sanitizer

H5

NDC: 64536-8920-1

NSF

Nonfood Compounds

Program Listed E3

Registration 136724

Net Contents

1 L / 1.06 U.S. Qt.

3358892

INGREDIENTS AND APPEARANCE

SOFT CARE FRAGRANCE FREE INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64536-8920
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64536-8920-1	1 L in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/22/2014

Labeler - Diversey, Inc. (018240817)

Establishment
Name	Address	ID/FEI	Business Operations
Kutol Products Company, Inc.		004236139	manufacture(64536-8920)