BLUZEN HAND SANITIZER MINT- ethyl alcohol gel

BLUZEN HAND SANITIZER MINT by

Drug Labeling and Warnings

BLUZEN HAND SANITIZER MINT by is a Otc medication manufactured, distributed, or labeled by Remcoda, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

INDICATIONS & USAGE

Uses ? hand sanitizer to help reduce bacteria on skin

Warnings

Flammable, keep away from fire/flame

For external use only

When using this product ? do not get into eyes. In case of contact, rinse eyes thoroughly with water

? do not inhale or ingest

Stop use and ask a doctor if irritation and redness develop

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

Directions

? place enough product in your palm to thoroughly cover your hands

? rub hands together briskly until dry

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

Other information

? Store below 110°F (43°C)

Inactive ingredients

glycerin, hydrogen peroxide, purified water, polyethylene glycol, carbomer copolymer, fragrance

QUESTIONS

Questions? 1-800-777-1603

SPL UNCLASSIFIED SECTION

CLEANSING FORMULA

KILLS 99.9% OF GERMS

MADE IN THE USA

SULFATE FREE PARABEN FREE

VEGAN, CRUELTY FREE

SHOPBLUZEN.COM

Distributed by: Remcoda, LLC, New York, NY, 10018

Packaging

INGREDIENTS AND APPEARANCE

BLUZEN HAND SANITIZER MINT 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79200-802
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79200-802-16	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/11/2020

Labeler - Remcoda, Llc (117130169)