ALCARE ANTISEPTIC HANDRUB- alcohol liquid

Alcare Antiseptic Handrub by

Drug Labeling and Warnings

Alcare Antiseptic Handrub 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, 70% 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 sanitizer to cover hands
• rub into skin
• no rinsing required

Inactive ingredients

aqua (water), glycerin, hydroxypropyl cellulose, panthenol, parfum (fragrance), trisodium dicarboxymethyl alaninate.

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

SCJ PROFESSIONAL
HEALTHCARE

Alcare®

NDC: 11084-035-27

Antiseptic Handrub Liquid

Excellent Moisturization

Net Contents: 1 Liter (33.8 fl oz)
SAP # 4000009648

REORDER #
ALCELV100
L-1448 RO

deb
SKIN CARE

INGREDIENTS AND APPEARANCE

ALCARE ANTISEPTIC HANDRUB 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-035
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
PANTHENOL (UNII: WV9CM0O67Z)
TRISODIUM DICARBOXYMETHYL ALANINATE (UNII: 784K2O81WY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-035-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/2021
2	NDC: 11084-035-18	370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/2021	12/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	505G(a)(3)	06/01/2021

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

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional CA Inc.		203765300	MANUFACTURE(11084-035)