ALCARE ENHANCED FOAMING HAND SANITIZER- alcohol liquid

Alcare Enhanced Foaming Hand Sanitizer by

Drug Labeling and Warnings

Alcare Enhanced Foaming 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]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

ETHYL ALCOHOL, 72% v/v

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) Behentrimonium Chloride, BIS-PEG-12 Dimethicone, Coco-Glucoside, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Glyceryl Oleate, PEG-200 Hydrogenerated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Propyl Alcohol.

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

SCJ PROFESSIONAL
A family company™

Alcare®
Enhanced

NDC: 11084-026-27

Foaming Hand Sanitizer

Excellent Moisturization

15
seconds

Fast-acting

CHG Compatible

REORDER #
107281

Manufactured for:
SC Johnson Professional
Charlotte, NC 28217
1-866-783-0422
www.scjp.com
Pat. www.scjp.com/patents
Made in Canada

1 Liter (33.8 fl oz)
SAP # 4000004994
L-1433 R0

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SKIN CARE

Open for
Drug Facts

INGREDIENTS AND APPEARANCE

ALCARE ENHANCED FOAMING HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
PROPYL ALCOHOL (UNII: 96F264O9SV)
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)
COCO GLUCOSIDE (UNII: ICS790225B)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
GLYCERYL OLEATE (UNII: 4PC054V79P)
PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-026-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2019
2	NDC: 11084-026-12	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2019
3	NDC: 11084-026-40	400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	10/01/2019

Labeler - SC Johnson Professional USA Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional CA Inc.		203765300	MANUFACTURE(11084-026)