Garnier Antiseptic Hand Sanitizer

Manufacturer
L'Oreal USA Products Inc
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:27:52

Label at a glance#

ProductGarnier Antiseptic Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

place enough product on hands to cover all surfaces. Rub hands together until dry. supervise chlildren 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

Alcohol 71% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or heat.

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • place enough product on hands to cover all surfaces. Rub hands together until dry.
  • supervise chlildren 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 ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, polyacryloyldimethyl taurate

Questions or comments?

OTC - QUESTIONS SECTION

1-800-370-1925

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-38549967-385-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
d1c20652-8eaf-475d-b5b1-b7fdbe46d344dff29645-0f9f-483f-af0b-8b5b40b5fe172022-06-30WarningsExact identifier
spl set id: dff29645-0f9f-483f-af0b-8b5b40b5fe17

Reported adverse events (FAERS/openFDA)#

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