SAN-EZ HAND SANITIZER- ethyl alcohol 70% gel

San-EZ Hand Sanitizer by

Drug Labeling and Warnings

San-EZ Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dental Technologies, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

70% v/v Ethyl Alcohol

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce microbes that potentially can cause disease.

• For use when soap and water are not available.

Warnings

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

Do not use

• on children less than 2 months of age
• on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occures. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

• Place enough product on hand to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30ºC (59-86ºF)
• Avoid freezing and excessive heat above 40ºC (104ºF)

Inactive ingredients

Water, Isopropyl Alcohol, Carbomer, Fragrance, Aminomethyl Propanol

Questions or comments?

Call 1-800-835-0885

Principal Display Panel

SAN-EZ™

Gel

Hand Sanitizer

Essened with Aloe & Shea

8 fl. oz. (236mL)

REF 033.0202.002

INGREDIENTS AND APPEARANCE

SAN-EZ HAND SANITIZER 
ethyl alcohol 70% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55346-3302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
DIMETHYL BENZYL CARBINOL (UNII: N95NCI59MI)
TRICYCLODECENYL PROPIONATE (UNII: 7MGZ636C87)
4-TERT-BUTYLCYCLOHEXYL ACETATE (UNII: 21EUM2B8UC)
BENZYL BENZOATE (UNII: N863NB338G)
CARBOMER 980 (UNII: 4Q93RCW27E)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
ACETYL CEDRENE (UNII: X6I62755AK)
ACETYL HEXAMETHYL TETRALIN (UNII: 360Q8Z01IP)
CYCLAMEN ALDEHYDE (UNII: 4U37UX0E1E)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
CITRAL (UNII: T7EU0O9VPP)
2-METHYL-4-PHENYL-2-BUTANOL (UNII: 9Y5UX90TZ4)
BENZYL ACETATE (UNII: 0ECG3V79ZJ)
LINALYL ACETATE (UNII: 5K47SSQ51G)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55346-3302-1	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - Dental Technologies, Inc. (148312838)

Registrant - Dental Technologies, Inc. (148312838)

Establishment
Name	Address	ID/FEI	Business Operations
Dental Technologies, Inc.		148312838	manufacture(55346-3302) , pack(55346-3302) , label(55346-3302)