FDA.reportPublic FDA data

Glow Town

Manufacturer
Glow Town Llc
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:25

Label at a glance#

ProductGlow Town
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other Information  ♦  Do not store above 105 °F  ♦  May discolour some fabrics. ♦  Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Medicinal Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Non Medicinal

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin,  Propylene Glycol, Carbomer, Aminomethyl Propanol,  Parfum

INDICATIONS & USAGE SECTION

Features  ♦  To decrease bacteria on the skin that could cause disease.

                ♦  Recommended for repeated use.

                ♦  Use anywhere without water.

DOSAGE & ADMINISTRATION SECTION

Directions  ♦ Wet hands thoroughly with product and rub until dry without wiping.

                  ♦ For children under 6, use only under adult supervision.

                  ♦ Not recommended for infants.

WARNINGS SECTION

Warning   ♦  For external use only-hands.

♦  Flammable. Keep away from heat and flame.

♦  Discontinue if skin becomes irritated and ask a doctor.

When using this product 

♦  Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

♦  Do not inhale or ingest.

♦  Avoid contact with broken skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

♦  Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

STORAGE AND HANDLING SECTION

Other Information  ♦  Do not store above 105°F  ♦  May discolour some fabrics.

♦  Harmful to wood finishes and plastics.

SPL UNCLASSIFIED SECTION

With Moisturizer and Vitamin E

Kills 99.99% of Germs

This product was not tested on animals.

Shelf life: 2 years

Production date: 04/15/2020

Address: Glow Town LLC

2656 Perth Street

DALLAS TX 25220

214-610-1178

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75047-186-012022-01-28C16284748780-1d6a99b39-d82a-a426-e053-dadaa90af4c2Glow Town INSTANT Hand Sanitizer Original
75047-186-032022-01-28C16284748780-1d6a99b39-d82a-a426-e053-dadaa90af4c2Glow Town INSTANT Hand Sanitizer Original
75047-186-052022-01-28C16284748780-1d6a99b39-d82a-a426-e053-dadaa90af4c2Glow Town INSTANT Hand Sanitizer Original

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75047-186-01Glow Town59 mL in 1 BOTTLE, PLASTICLIQUID591
75047-186-03Glow Town236 mL in 1 BOTTLE, PLASTICLIQUID2361
75047-186-05Glow Town500 mL in 1 BOTTLE, PUMPLIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75047-186GLOW TOWN (ETHYL ALCOHOL) LIQUID [GLOW TOWN LLC]1Legacy NDC, 3 package rows20200502_f2ac0dba-e969-4cd3-9f33-df9b993099ac.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75047-18675047-186-01, 75047-186-03, 75047-186-05

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
01bd3142-7e4b-403e-ae21-5258cb37e519f2ac0dba-e969-4cd3-9f33-df9b993099ac2020-04-29WarningsExact identifier
spl id: 01bd3142-7e4b-403e-ae21-5258cb37e519
spl set id: f2ac0dba-e969-4cd3-9f33-df9b993099ac

Reported adverse events (FAERS/openFDA)#

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