FDA.reportPublic FDA data

Hands Free Sanitizer Gel

Manufacturer
AG Hair Ltd
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:45:20

Label at a glance#

ProductHands Free Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to help decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Distribute thoroughly over front and back of entire hands including between fingers and thumbs. Rub together and air dry. Reapply as required. Use when soap and water are not immediately available and after coming into contact with any potential germ source.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 73% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin that could cause disease.

  • Recommended for repeated use.

Warnings:

WARNINGS SECTION

Flammable. Do not store over 110°F (43°C) Keep away from fire or flame. For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if 

OTC - STOP USE SECTION

irritation or rash appears and lasts.

Keep this and all drugs out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For adults and adolescents over the age of 12. If swallowed, call a poison control centre or get medical help right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Distribute thoroughly over front and back of entire hands including between fingers and thumbs. Rub together and air dry. Reapply as required.

  • Use when soap and water are not immediately available and after coming into contact with any potential germ source.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aqua (Water/Eau), Glycerin, Propanediol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate (Vitamin E), Polysorbate 20, Carbomer, Aminomethyl Propanol, Fragrance/Parfum (Natural).

Questions?

OTC - QUESTIONS SECTION

1-866-924-4247

Package Labeling: 46324-2500-3

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HS355HS355

Package Labeling: 46324-2500-5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HS59HS59

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46324-250046324-2500-3, 46324-2500-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
POLYSORBATE 207T1F30V5YHIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALCOHOL3K9958V90MACTIB

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
ef3f996c-33b1-ef0e-e053-2a95a90a0fe0870e2c24-8edf-4382-8697-4b9a2ec1f6772022-12-07WarningsExact identifier
spl id: ef3f996c-33b1-ef0e-e053-2a95a90a0fe0
spl set id: 870e2c24-8edf-4382-8697-4b9a2ec1f677

Reported adverse events (FAERS/openFDA)#

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