SANNYTIZE HAND SANITIZER- alcohol gel

SannyTize Hand Sanitizer by

Drug Labeling and Warnings

SannyTize Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                         Purpose

Ethyl Alcohol 0.62%                   Antiseptic Handwash

WARNINGS

• For external use only
• Flammable, keep away from fire and flame
• Do not use in or near the eyes
• When using this product avoid contact with eyes. In case of eye contact, rinse with water to remove.
• Stop use and ask a doctor if irritation andredness develops

PURPOSE

An antiseptic handwash.

INDICATIONS & USAGE

Cleaning and antiseptic cleansing of hands and skin.

DOSAGE & ADMINISTRATION

• Wet hands thoroughly with product and allow to dry without wiping

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.

INACTIVE INGREDIENTS

Inactive ingredients: Water, Glycerin, Propylene glycol, Carbomer, Triethanolamine, Aloe barbadensis juice, Fragrance

PRINCIPAL DISPLAY PANEL

Dynarex SannyTize Hand Sanitizer

hand sanitizer.jpg

INGREDIENTS AND APPEARANCE

SANNYTIZE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-317
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-317-01	29.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2017
2	NDC: 67777-317-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2017
3	NDC: 67777-317-03	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2017
4	NDC: 67777-317-04	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2017
5	NDC: 67777-317-05	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/25/2017
6	NDC: 67777-317-06	1.035 mL in 1 PACKET; Type 0: Not a Combination Product	04/25/2017
7	NDC: 67777-317-07	1.035 mL in 1 PACKET; Type 0: Not a Combination Product	04/25/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/25/2017

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)