Hand Sanitizer Moisturizing Gel 500mL

Manufacturer
Lafang China Co.,Ltd
Effective date
2020-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:37:02

Label at a glance#

ProductCOCOEARTH HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Take a thumbnail size drop on your palm and rub your hands together covering all surfaces of both hands, including between your fingers and up around your fingertips and nails. Rub hands together until completely dry.

Storage and handling

Store in a cool dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75% v/v. Purpose: Antiseptic

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine

INDICATIONS & USAGE SECTION

Use Hand sanitizer to effective at eliminating 99.9% of many common harmful germs and bacteria.

OTC - PURPOSE SECTION

Antiseptic

Directions for Use

DOSAGE & ADMINISTRATION SECTION

Take a thumbnail size drop on your palm and rub your hands together covering all surfaces of both hands, including between your fingers and up around your fingertips and nails. Rub hands together until completely dry.

Warnings

WARNINGS SECTION

Keep away from a naked flame, source of heat, open live electric wire, etc.

Do not use

OTC - DO NOT USE SECTION

Not for injection and do not use in body cavities.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - STOP USE SECTION

If irritation occurs, wash affected area and discontunue use.

OTC - WHEN USING SECTION

Avoid contact with eyes. Do not swallow.

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool dry place.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 mL NDC: 74612-004-01

PDPPDP

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
74612-00474612-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
a824f1b9-6b1a-3bc7-e053-2a95a90a0595a2bd3b27-12fc-d3ae-e053-2a95a90aef412020-06-15WarningsExact identifier
spl set id: a2bd3b27-12fc-d3ae-e053-2a95a90aef41

Reported adverse events (FAERS/openFDA)#

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