EMU HAND SANITIZER MIST ORANGE BLOSSOM- alcohol spray

EMU Hand Sanitizer Mist Orange Blossom by

Drug Labeling and Warnings

EMU Hand Sanitizer Mist Orange Blossom by is a Otc medication manufactured, distributed, or labeled by EVERYONE MUST USE, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Purpose

Antiseptic, Hand Sanitizer

Drug Facts

• Active Ingredient: Purpose
• Ethyl Alcohol 62%: Antiseptic

Uses

Hand sanitizer to help reduce bacteria that can potentially cause disease. For use when soap and water are not available.

Warnings

For external use only. | Flammable. | Keep away from heat or flame. | Contents under pressure.

Do not use

Do not use on children less than 2 months of age. Do not use on open skin wounds.

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

​Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 15°-30° C (59°-86°F)

Inactive ingredients

Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Purified Water, Tocopheryl Acetate

Questions or comments?

1-800-250-4643

Package Label - Principal Display Panel

Net Wt 2.2 FL OZ (62.4g) NDC: 80464-1005-1

INGREDIENTS AND APPEARANCE

EMU HAND SANITIZER MIST ORANGE BLOSSOM 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80464-1005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80464-1005-1	62.4 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/23/2020

Labeler - EVERYONE MUST USE, LLC (117650280)