SANNYTIZE HAND SANITIZER WIPE- alcohol gel
Dynarex Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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1306 Dynarex SannyTize Hand Sanitizer Wipes NDC 67777-320-01

ACTIVE INGREDIENT

Active Ingredient Purpose

Ethyl Alcohol 70% Antiseptic Wipe

WARNINGS

For external use only
Flammable, keep away from fire and flame
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

Antiseptic handwash

INDICATIONS & USAGE

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

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, Diazolidinyl urea, Aloe barbadensis leaf juice, Polysorbate 20, Carbomer, Tocopherol acetate, Methylparaben, Propylparaben, Triethanolamine

PRINCIPAL DISPLAY PANEL

1306 IN Master Dynarex SannyTizer HandSanitizing Wipes

Sannywipe.jpg

SANNYTIZE HAND SANITIZER WIPE
alcohol gel

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

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
METHYLPARABEN (UNII: A2I8C7HI9T)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:67777-320-02	1620 in 1 CASE	04/25/2017
1	NDC:67777-320-01	135 in 1 CANISTER
1		3.42 mL in 1 PATCH; Type 0: Not a Combination Product

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

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)