Alcare® Elevate Antiseptic Handrub

Alcare Elevate Antiseptic Handrub by

Drug Labeling and Warnings

Alcare Elevate 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]

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

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Alcare® Elevate Antiseptic Handrub

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

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 Product10/15/202012/31/2025
2NDC: 11084-034-18370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/15/202012/31/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM00310/15/202012/31/2025
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional CA Inc.203765300MANUFACTURE(11084-034)

Revised: 12/2024
Document Id: d6795a2c-b8be-4fb9-af45-e4bd5addc16a
Set id: e3dbbb51-509c-41fe-afdb-a09688272b49
Version: 2
Effective Time: 20241213