DAWNMIST ALCOHOL HAND SANITIZER- alcohol gel

DawnMist Alcohol Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antibacterial Agent

Use:

For hand washing to decrease bacteria on skin.

Warnings

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

Do not use in the eyes ■ In rare instances of irritation,
discontinue use if irritation and redness develop ■ If
condition persists for more than 72 hours, consult a
physician

Keep out of reach of children.

■ If swallowed, contact a physician or poison center ■ Use only as directed

Directions:

To decrease bacteria on skin, apply a small amount to palm. Briskly rub covering hands with product until dry.

Inactive Ingredients:

Water, Glycerin, Propylene Glycol, DMDM Hydantoin, Aminomethyl Propanediol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Vera Leaf Extract, Tocopherol

Package Label

NDC: 65517-1007-3

DawnMist

Handwashing

Hand Sanitizer

Citrus Scent

Kills 99.99% of Germs

4 FL. OZ. (118ml)

INGREDIENTS AND APPEARANCE

DAWNMIST ALCOHOL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65517-1007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DMDM HYDANTOIN (UNII: BYR0546TOW)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-1007-1	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	01/14/2013
2	NDC: 65517-1007-2	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/14/2013
3	NDC: 65517-1007-3	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/14/2013
4	NDC: 65517-1007-4	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/14/2013
5	NDC: 65517-1007-5	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/14/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/14/2013

Labeler - Dukal Corporation (791014871)