SANNYTIZE HAND SANITIZER WIPE- alcohol gel

SannyTize Hand Sanitizer Wipe by

Drug Labeling and Warnings

SannyTize Hand Sanitizer Wipe 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 70%                   Antiseptic Wipe

WARNINGS

• For external use only
• Flammable, keep away from fire and 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 develops

PURPOSE

An antiseptic wipe.

INDICATIONS & USAGE

Cleaning and antiseptic cleansing of hands and skin.

DOSAGE & ADMINISTRATION

• To start feed: Remove cover and discard seal from container, From center of toweled roll , pull up wipe corner; tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover.Pull through about one inch. Replace cover,Pull out wipes as needed and snap off at 90°angle. Keep cap closed to prevent moisture loss.
• Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry.
• If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, Sanitize with a second wipe.
• Discard after single use.

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, Diazolidinyl urea, Aloe barbadensis juice, Polysorbate 20, Carbomer, Tocopherol acetate, Citric acid, Methylparaben, Propylparaben, Fragrance

PRINCIPAL DISPLAY PANEL

Dynarex SannyTize Sanitizing Wipe

Sannywipe.jpg

INGREDIENTS AND APPEARANCE

SANNYTIZE HAND SANITIZER WIPE 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-320
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID ACETATE (UNII: DSO12WL7AU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
METHYLPARABEN (UNII: A2I8C7HI9T)
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-320-01	135 in 1 CANISTER	04/25/2017
1		3.42 mL in 1 PATCH; 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	04/25/2017

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)