FDA.reportPublic FDA data

Thompson Hand Sanitizer

Manufacturer
Thompson | Unifirst First Aid Corpration | Medique Products
Effective date
2025-09-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:12:45

Label at a glance#

ProductThompson Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

  • for handwashing to reduce bacteria on skin without soap and water
  • recommended for repeated use

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use in the eyes. If this happens, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops and persists for 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • wet hands and wrists thoroughly with product and allow to dry without wiping
  • children under 6 years of age should be supervised when using this product

OTHER SAFETY INFORMATION

  • store at 59-86°F (15-30°C)
  • tamper evident. Do not use if packet is torn, cut or opened.

INACTIVE INGREDIENT SECTION

aloe vera. carbomer D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

OTC - QUESTIONS SECTION

877.506.4291

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND SANITIZER

ETHYL ALCOHOL 66.5%

WITH ALOE VERA

NET WT 0.9 G (1/32 OZ) PACKETS

25 /BOX THOMPSON

SAFETY WORKS ǀ BUSINESS THRIVES ᵀᴹ

Thompson Hand SanitizerThompson Hand Sanitizer

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73408-513-73Thompson Hand Sanitizer0.00168 L in 1 PACKETGEL0.001685
73408-513-73Thompson Hand Sanitizer25 in 1 BOXGEL255

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
73408-51373408-513-73

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOEV5VD430YW9IACT
D&C YELLOW NO. 1035SW5USQ3GIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
D&C GREEN NO. 58J6RDU8L9XIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT

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 SanitizerALCOHOL GELThompson06beaf35-f814-bf9b-e063-6294a90aec8c2025-09-08WarningsExact identifier
ndc (package): 73408-513-73
ndc (product): 73408-513
ndc11 (package): 73408051373
spl id: 3e4f91aa-aee1-f154-e063-6394a90a951d
spl set id: 06beaf35-f814-bf9b-e063-6294a90aec8c

Reported adverse events (FAERS/openFDA)#

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