EMU HAND SANITIZER MIST OCEAN SURF- alcohol spray

EMU Hand Sanitizer Mist Ocean Surf by

Drug Labeling and Warnings

EMU Hand Sanitizer Mist Ocean Surf 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

• Active Ingredient: Purpose
• Alcohol 80% v/v.: Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially can 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 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 using 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 to avoid swallowing.

Other information

Store between 15°-30° C (59°-86°F)

Inactive ingredients

Aloe, Fragrance, Glycerin, Purified Water, Vitamin E

Questions or comments?

1-800-250-4643

Package Label - Principal Display Panel

Net Wt 2.2 FL OZ (62.4g) NDC: 80464-1002-1

INGREDIENTS AND APPEARANCE

EMU HAND SANITIZER MIST OCEAN SURF 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80464-1002
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)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80464-1002-1	62.4 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/21/2020

Labeler - EVERYONE MUST USE, LLC (117650280)