FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
Music City Laboratories, Llc
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:15:12

Label at a glance#

ProductInstant Hand Sanitizer
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 Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%.

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For rinse-free hand sanitizing to remove 99.9% bacteria on skin.

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and persist.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

OTHER SAFETY INFORMATION

Store under 105°F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylates Copolymer, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

Principal Display Panel – 8 fl oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

music city
LABORATORIES

Kills
99.9%
of Germs

INSTANT GEL
Hand
Sanitizer

moisturizing formula with aloe

8 fl oz (240 ml)

Principal Display Panel – 8 fl oz Bottle Label
Principal Display Panel – 8 fl oz Bottle Label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73652-10173652-101-01, 73652-101-02, 73652-101-03, 73652-101-04, 73652-101-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
Butyl Acrylate/Methyl Methacrylate/Methacrylic Acid Copolymer (18000 MW)JZ1374NL9EIACT
Aloe Vera LeafZY81Z83H0XIACT
GlycerinPDC6A3C0OXIACT
.Alpha.-Tocopherol Acetate9E8X80D2L0IACT
Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked)59TL3WG5COIACT
AminomethylpropanolLU49E6626QIACT

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
c3456238-3a4a-45b7-b312-d90fcecf3eb8fe7bf3a0-d492-4de6-9ff3-ee4eb88c814b2023-01-16WarningsExact identifier
spl set id: fe7bf3a0-d492-4de6-9ff3-ee4eb88c814b

Reported adverse events (FAERS/openFDA)#

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