FDA.reportPublic FDA data

Thompson Hand Sanitizer

Manufacturer
Thompson | Unifirst First Aid Corporation
Effective date
2024-01-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:07:31

Label at a glance#

ProductThompson Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 62% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic handwash

INDICATIONS & USAGE SECTION

Uses

  • for hand washing to decrease bacteria on the skin
  • recommended for repeated use

WARNINGS SECTION

Warnings

  • For external use only
  • Flammable, keep away from fire or flames

OTC - WHEN USING SECTION

When using this product

  • do not use in or around the eyes
  • in case of contact with eyes, rinse eyes throroughly with water

OTC - STOP USE SECTION

Stop use ans ask a doctor if

  • irritation or rash develops
  • condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6 years of age, use only under adult supervision

OTHER SAFETY INFORMATION

Other information

  • store at 59-77ºF (15-25ºC)
  • may discolor certain fabrics or surfaces
  • tamper evident. Do not use if packet is torn, cut or opened
  • you may report a serious adverse reaction to this product to 877.506.4291

INACTIVE INGREDIENT SECTION

Inactive ingredients

acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, fragrance, PEG-60 almond glycerides, propylene glycol, tocopheryl acetate, triisopropanolamine, water

OTC - QUESTIONS SECTION

Questions or comments? 877.506.4291

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Thompson

Hand Sanitizer

Ethyl Alcohol 62%

With Aloe Vera

Net WT 0.9 g (1/32 OZ) Packets

25/Box

Thompson

Safety Works | Buisness Thrives™

ThompsonThompson

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73408-512-73Thompson Hand Sanitizer25 in 1 BOXGEL253
73408-512-73Thompson Hand Sanitizer0.9 mL in 1 PACKETGEL0.93

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73408-512THOMPSON HAND SANITIZER (ETHYL ALCOHOL) GEL [THOMPSON]3Current NDC, Legacy NDC, 2 package rows20240118_deada606-8a82-9eeb-e053-2a95a90a9e6d.zip

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
73408-51273408-512-73

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
WATER059QF0KO0RIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
TRIISOPROPANOLAMINEW9EN9DLM98IACT
ALCOHOL3K9958V90MACTIB
PEG-60 ALMOND GLYCERIDES4Y0E651N0FIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT

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
Thompson Hand SanitizerETHYL ALCOHOLThompsondeada606-8a82-9eeb-e053-2a95a90a9e6d2024-01-16WarningsExact identifier
ndc (package): 73408-512-73
ndc (product): 73408-512
ndc11 (package): 73408051273
spl id: 0f168fab-9ef4-4a8b-e063-6294a90adc65
spl set id: deada606-8a82-9eeb-e053-2a95a90a9e6d

Reported adverse events (FAERS/openFDA)#

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