FDA.reportPublic FDA data

LOreal Antiseptic Hand Sanitizer

Manufacturer
L'Oreal USA Products Inc
Effective date
2021-05-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:44:33

Label at a glance#

ProductLOreal Antiseptic Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

put enough product in your palm to cover hands. Rub hands together until dry. supervise chlildren under 6 years of age 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 decrease bacteria on the skin

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

  • put enough product in your palm to cover hands. Rub hands together until dry.
  • supervise chlildren under 6 years of age 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

Toll-free number 1-888-448-9617

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

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
49967-86849967-868-01, 49967-868-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S)F01RIY4371IACT

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
228e264d-7c9e-4937-a326-d6141df3a0f0d2c32b09-396f-40fa-aae2-508420ba7cb02022-06-21WarningsExact identifier
spl set id: d2c32b09-396f-40fa-aae2-508420ba7cb0

Reported adverse events (FAERS/openFDA)#

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