MICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM

Manufacturer
CARONLAB AUSTRALIA PTY LTD
Effective date
2022-01-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:21

Label at a glance#

ProductMICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

hand sanitizer to decrease bacteria on the skin recommended for repeated use for use when soap and water are not available

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

store between 15-30°C (59-86°F) avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to decrease bacteria on the skin
  • recommended for repeated use
  • for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use

  • in children less than 2 months of age
  • on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

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

  • wet hands thoroughly with product and allow to dry without wiping
  • supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

  • store between 15-30°C (59-86°F)
  • avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients cocamidopropyl propylene glycol-dimonium chloride phosphate, water

OTC - QUESTIONS SECTION

Questions? +1-305-985-7803
You may also report serious side effects to this phone number.
Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

  • decreases bacteria on the skin
  • no water required
  • non drying

Contains: Benzalkonium Chloride 0.1% w/v

Manufactured by:

Caronlab Australia Pty Ltd

148-150 Victoria St,

North Geelong, VIC, Australia 3215

Product of Australia

www.caronlab.com.au

Phone: + 1-305-985-7803

Made in Australia   Dispose of thoughtfully   Vegan friendly   Certified Cruelty Free

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN2
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD2
1038799benzalkonium chloride 0.1 % Topical FoamSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77277-633-682024-01-30C16284748780-11030e365-61af-111a-e063-dadaa90a10e2micro defence ANTISEPTIC HAND SANITIZER FOAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77277-633-68MICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM200 mL in 1 BOTTLELIQUID2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77277-633MICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM (BENZALKONIUM CHLORIDE) LIQUID [CARONLAB AUSTRALIA PTY LTD]2Legacy NDC, 1 package rows20220121_c1456c3b-bfcf-439f-b1fe-3533489cd722.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77277-63377277-633-68

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
f664d57a-5cb9-419a-b9b0-09efd719b647c1456c3b-bfcf-439f-b1fe-3533489cd7222022-01-19WarningsExact identifier
spl id: f664d57a-5cb9-419a-b9b0-09efd719b647
spl set id: c1456c3b-bfcf-439f-b1fe-3533489cd722

Reported adverse events (FAERS/openFDA)#

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