ALCARE ELEVATE ANTISEPTIC HANDRUB- alcohol liquid 
SC Johnson Professional USA, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Alcare® Elevate Antiseptic Handrub

Drug Facts

Active ingredient

Ethyl Alcohol, 70% v/v

Purpose

Antibacterial

Uses

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

Inactive ingredients

Aqua (Water), Glycerin, Hydroxypropyl Cellulose, Panthenol, Parfum (Fragrance), Trisodium Dicarboxymethyl Alaninate.

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

Alcare®

Antiseptic Handrub
Elevate

SCJ PROFESSIONAL
HEALTHCARE

NDC 11084-034-27

Excellent Moisturization

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

REORDER #
ALCELV100

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SKIN CARE

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
ALCARE ELEVATE ANTISEPTIC HANDRUB 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-034
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
DEXPANTHENOL (UNII: 1O6C93RI7Z)  
TRISODIUM DICARBOXYMETHYL ALANINATE (UNII: 784K2O81WY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-034-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/15/2020
2NDC:11084-034-18370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/15/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E10/15/2020
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional CA Inc.203765300MANUFACTURE(11084-034)

Revised: 9/2020
Document Id: f25ddc01-c64e-4dfd-8877-206b1f7059ac
Set id: e3dbbb51-509c-41fe-afdb-a09688272b49
Version: 1
Effective Time: 20200929
 
SC Johnson Professional USA, Inc.