FDA.reportPublic FDA data

A La Maison Hand Sanitizer

Manufacturer
A La Maison De Provence LLC
Effective date
2020-11-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:05:08

Label at a glance#

ProductA La Maison Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants

Storage and handling

Store at 68-77 o F. (20-25 o C) May discolor some fabrics Harmful to wood finishes and plastic

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

A La Maison

Hand Sanitizer

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

Do not use

  • around eyes
  • in ears and mouth

When using this product

OTC - WHEN USING SECTION

When using this product

  • Keep out of eyes. In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

OTC - STOP USE SECTION

  • Stop use and ask a doctor

if irritation or redness develops

Keep out of reach of children

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.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

  • Store at 68-77 oF. (20-25 oC)
  • May discolor some fabrics
  • Harmful to wood finishes and plastic

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, acrylates copolymer, glycerin, hydrogen peroxide, triethanolamine, aloe barbadensis leaf juice powder.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

300 mL NDC: 74628-0010-3

LabelLabel

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
74628-001074628-0010-3

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOEV5VD430YW9IACT

Source Document#

Source XML · Source PDF

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
d57f6ee2-5f55-b704-e053-2995a90ab098a4684fa8-aa4f-0ad4-e053-2a95a90ad5392022-01-13WarningsExact identifier
spl set id: a4684fa8-aa4f-0ad4-e053-2a95a90ad539

Reported adverse events (FAERS/openFDA)#

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