THOMPSON HAND SANITIZER- ethyl alcohol gel

Thompson Hand Sanitizer by

Drug Labeling and Warnings

Thompson Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Thompson, Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Ethyl Alcohol 62% v/v

PURPOSE

Purpose

Antiseptic handwash

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

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

WHEN USING

When using this product

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

STOP USE

Stop use ans ask a doctor if

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

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

Inactive ingredients

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

QUESTIONS

Questions or comments? 877.506.4291

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™

INGREDIENTS AND APPEARANCE

THOMPSON HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73408-512
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)
PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73408-512-73	25 in 1 BOX	08/01/2022	04/30/2028
1		0.9 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/01/2022	04/30/2028

Labeler - Thompson (080998015)

Registrant - Unifirst First Aid Corporation (832947092)