FDA.reportPublic FDA data

Lafco New York Hand Sanitizer Champagne

Manufacturer
GFL SA
Effective date
2022-06-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:59:00

Label at a glance#

ProductLafco New York Hand Sanitizer Champagne
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 73.2%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

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

wet hands thoroughly with product and allow to dry without wiping.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Parfum (fragrance), glycerin, aloe barbadensis leaf juice, acrylates/c-10-30 alkyl acrylate crosspolymer, triethanolamine, t-butyl alcohol, propylene glycol, ethylene brassylate, citric acid, ginkgo biloba extract, sodium benzoate, potassium sorbate.

Package Labeling:380ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

380mL Label380mL LabelDrug FactsDrug Facts

Package Labeling:100ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100mL100mL

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77513-00777513-007-01, 77513-007-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
TERT-BUTYL ALCOHOLMD83SFE959IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
TROLAMINE9O3K93S3TKIACT
GINKGO19FUJ2C58TIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB
SODIUM BENZOATEOJ245FE5EUIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ETHYLENE BRASSYLATE9A87HC7RODIACT

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
e1e66d97-d1a1-41fe-e053-2995a90ae883bb7a5af5-e3b9-9696-e053-2995a90a828a2022-06-20WarningsExact identifier
spl id: e1e66d97-d1a1-41fe-e053-2995a90ae883
spl set id: bb7a5af5-e3b9-9696-e053-2995a90a828a

Reported adverse events (FAERS/openFDA)#

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