ALCARE EXTRA HAND SANITIZER- alcohol solution

Alcare Extra Hand Sanitizer by

Drug Labeling and Warnings

Alcare Extra Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., SC Johnson Professional CA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ETHYL ALCOHOL, 80% w/w

Purpose

Antibacterial

Uses

for hand sanitizing to reduce bacteria on the skin

Warnings

For external use only

Flammable:

Keep away from fire or flame.

When using this product

avoid contact with eyes. In case of eye contact, flush with water.

Keep out of reach of children.

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

Directions

apply foaming sanitizer to cover hands

rub into skin

no rinsing required

Inactive ingredients

AQUA (WATER), BIS-PEG-12 DIMETHICONE, CITRIC ACID, COCO-GLUCOSIDE, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERYL OLEATE, PANTHENOL, PEG-200 HYDROGENATED GLYCERYL PALMITATE, PEG-7 GLYCERYL COCOATE

PRINCIPAL DISPLAY PANEL

Alcare® Extra
NDC: 11084-006-27
Hand Sanitizer
Foaming Antiseptic Handrub
Excellent Moisturization
Fast-acting
CHG Compatible
1 Liter (33.8 fl oz) (1.05 qt)
DebMed USA, LLC. Charlotte, NC 28217 1-866-783-0422 www.debmed.com
Made in Canada. L-1398 R0
Open for
Drug Facts
Perfume-free
Dye-free
No water required
Kills 99.999% of many types of common germs
Meets food code hand sanitizer criteria (Section 2-301.16) published by the FDA
US Patents 5,445,288 & 6,082,586
Worldwide Patent Pending.
Stock #: 101561

INGREDIENTS AND APPEARANCE

ALCARE EXTRA HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCO GLUCOSIDE (UNII: ICS790225B)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
GLYCERYL OLEATE (UNII: 4PC054V79P)
PANTHENOL (UNII: WV9CM0O67Z)
PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-006-01	47 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2017
2	NDC: 11084-006-40	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2017
3	NDC: 11084-006-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2017
4	NDC: 11084-006-12	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2017

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

Registrant - SC Johnson Professional USA, Inc. (078805627)

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional CA Inc.		203765300	manufacture(11084-006)