CLINISHIELD INSTANT HAND SANITIZER- ethyl alcohol liquid

Clinishield Instant Hand Sanitizer by

Drug Labeling and Warnings

Clinishield Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., Aphena Pharma Solutions-Maryland LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol (62%)

Purpose

Hand Antiseptic

Uses

Hand antiseptic to decrease bacteria on the skin.

Flammable

For external use only

Avoid contact with eyes.  In case of accidental eye contact, flush eyes thoroughly with water.

Stop use and ask doctor if

Skin or eye irritation persists for more than 72 hours.

Keep out of reach of children.

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

Directions

Dispense an adequate amount (approx. 5 mL), rubbing over all surfaces of both hands for at least 15 seconds.  Allow to dry without wiping.

Inactive Ingredients

Deionized Water, Isopropanol, Hydrogenated Starch Hydrolysate, Carbomer, THP Ethylenediamine, Fragrance.

PRINCIPAL DISPLAY PANEL

NDC: 11084-941-50
NPN 80023556
Instant Hand Sanitizer
NO RINSING
DÉSINFECTANT
Instantané Pour Les Mains
SANS RINÇAGE
CliniShield®
NET CONTENTS 16 FL OZ
CONTENU NET 473 ml
Stock #33245
No.De STOCK 33245
Distributed by/Distribué par
Deb Canada
Waterford,ON N0E1Y0
1-888-332-7627
deb
Manufactured in U.S.A./Fabriquée aux É.-U.
Deb USA, Inc.
Charlotte, NC, 28217
1-800-248-7190 / www.stokoskincare.com

INGREDIENTS AND APPEARANCE

CLINISHIELD INSTANT HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-941
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYL ALCOHOL (UNII: 96F264O9SV)
HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)
CARBOMER 940 (UNII: 4Q93RCW27E)
EDETOL (UNII: Q4R969U9FR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-941-50	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014	12/31/2021
2	NDC: 11084-941-22	1600 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014	12/31/2021
3	NDC: 11084-941-30	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014	12/31/2022
4	NDC: 11084-941-11	118.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014	12/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2014	12/31/2022

Labeler - SC Johnson Professional USA, Inc. (607378015)

Registrant - SC Johnson Professional USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Aphena Pharma Solutions-Maryland LLC		829739833	manufacture(11084-941)