SANNYTIZE HAND SANITIZER- hand sanitizer 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

Ethyl Alcohol 70%

Purpose

Antiseptic Handwash

Use

• For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only

Flammable. Keep away from fire or flame

Do not use

in 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 and redness develop.

Keep out of reach of children.

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

Directions

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

Other Information

• Do not store above 110°F
• May discolor some fabrics

Inactive Ingredients

Aloe Vera Leaf, Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked), Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine, Water

Labels

INGREDIENTS AND APPEARANCE

SANNYTIZE HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-010
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
WATER (UNII: 059QF0KO0R)
MALTODEXTRIN (UNII: 7CVR7L4A2D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-010-01	144 in 1 CASE	11/01/2019
1		24 in 1 BOX
1		29.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 67777-010-02	144 in 1 CASE	11/01/2019
2		24 in 1 BOX
2		59 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 67777-010-03	96 in 1 CASE	11/01/2019
3		24 in 1 BOX
3		118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 67777-010-04	48 in 1 CASE	11/01/2019
4		236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 67777-010-05	12 in 1 CASE	11/01/2019
5		473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6	NDC: 67777-010-06	1728 in 1 CASE	11/01/2019
6		144 in 1 BOX
6		1.01 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 not final	part333A	11/01/2019

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)