SOFT CARE IMPACT FOAM ALCOHOL FOAM INSTANT HAND SANITIZER- alcohol liquid

Soft Care Impact Foam Alcohol Foam Instant Hand Sanitizer by

Drug Labeling and Warnings

Soft Care Impact Foam Alcohol Foam Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Diversey, Inc., Diversey Canada, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Alcohol 76% v/v

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

To decrease bacteria on the skin.

Recommended for repeated use.

WARNINGS

Warnings

Flammable. Keep away from fire or flame.

For external use only.

Do not ingest.

Do not use in the eye.

When using this product do not get into 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 reach of children.

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

DOSAGE & ADMINISTRATION

Directions

Apply 0.4-1 ml into hands.

Rub product vigorously over hands covering all surfaces.

Allow to air dry - do not rinse.

REFERENCES

Other information

EMERGENCY PHONE: 1-800-851-7145

See SDS MS0301541

FOR COMMERCIAL USE.

See container for Lot Code and Expiry Date.

Store in a cool dry place.

INACTIVE INGREDIENT

Inactive ingredients

Water, PEG-10 Dimethicone, Glycerin, Isopropyl myristate

QUESTIONS

Questions or comments?

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

www.diversey.com

PRINCIPAL DISPLAY PANEL

NDC: 64536-8068-2

Diversey

SoftCare Impact Foam

Alcohol Foam Instant Hand Sanitizer

For commercial use

USDA CERTIFIED BIOBASED PRODUCT Product 96%

U

(L) Exp.

NSF

Nonfood Compounds

Program Listed E3

Registration # 153923

UL ECOLOGO

Net Contents

1.2 L/1.27 U.S. Qt.

SKU: 100907873

INGREDIENTS AND APPEARANCE

SOFT CARE IMPACT FOAM ALCOHOL FOAM INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64536-8068
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	76 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64536-8068-2	1.2 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/15/2016
2	NDC: 64536-8068-9	208 L in 1 DRUM; Type 0: Not a Combination Product	04/14/2020
3	NDC: 64536-8068-3	3.785 L in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/15/2016

Labeler - Diversey, Inc. (018240817)

Establishment
Name	Address	ID/FEI	Business Operations
Diversey Canada, Inc		249266974	manufacture(64536-8068)