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]

DawnMist Alcohol Hand Sanitizer

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

To decrease bacteria on the skin that could cause disease

Warning

For external use only

Flammable, keep away from fire or flame.

When using this product

Keep out of eyes, ears and mouth. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor if

irritation or redness develops

Keep out of reach of children

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

Directions

wet hands thoroughly with products and allow to dry without wiping.

for children under 6, use only under adult supervision

Other Information

Avoid freezing and excessive heat above 104°F

Inactive Ingredients

Acrylates/C10-30Alkyl Acrylate Cross Polymer, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine, Water

Principle Display Panel

NDC: 65517-1023-1

DawnMist ®

Hand Sanitizer

Drug Facts

Active Ingredient Purpose

Ethyl alcohol 62%.........Antiseptic

REF HS8004

4 FL. OZ. (118 ml)

INGREDIENTS AND APPEARANCE

DAWNMIST ALCOHOL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65517-1023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-1023-1	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/09/2020

Labeler - Dukal Corporation (791014871)