Alcare Elevate Antiseptic Handrub

Manufacturer
SC Johnson Professional USA, Inc. | SC Johnson Professional CA Inc.
Effective date
2024-12-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:45:48

Label at a glance#

ProductAlcare Elevate Antiseptic Handrub
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

for hand sanitizing to reduce bacteria on the skin

Dosage and administration

apply sanitizer to cover hands rub into skin no rinsing required

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • for hand sanitizing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable: Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply sanitizer to cover hands
  • rub into skin
  • no rinsing required

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

deb
SKIN CARE

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11084-034ALCARE ELEVATE ANTISEPTIC HANDRUB (ALCOHOL) LIQUID [SC JOHNSON PROFESSIONAL USA, INC.]2Legacy NDC20241218_e3dbbb51-509c-41fe-afdb-a09688272b49.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11084-03411084-034-27, 11084-034-18

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d6795a2c-b8be-4fb9-af45-e4bd5addc16ae3dbbb51-509c-41fe-afdb-a09688272b492024-12-13WarningsExact identifier
spl id: d6795a2c-b8be-4fb9-af45-e4bd5addc16a
spl set id: e3dbbb51-509c-41fe-afdb-a09688272b49

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.