MIRACLE BRANDS HAND SANITIZER- alcohol free hand sanitizer liquid

Miracle Brands Hand Sanitizer by

Drug Labeling and Warnings

Miracle Brands Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Global Health Solutions DBA Turn Therapeutics, Westwood Labs, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Drug Facts

Purpose

Antimicrobial

Uses

• for hand sanitizing to decrease bacteria on the skin
• recommended for repeated use

Warnings

For external use only

STOP USE

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• spray a small amount of liquid into the palm of hand
• rub thoroughly over all surfaces of both hands
• rub hands together briskly until dry

Inactive Ingredients

water, didecyldimonium chloride, propylene glycol, methylparaben, diazolidinyl urea, propylparaben, cocamidopropylamine oxide, allantoin, cocamidopropyl betaine, cetrimonium chloride, triethanolamine, citric acid

Miracle Brands® POWERED BY CURX®

HAND

SANITIZING

LIQUID SPRAY

KILLS 99%

OF GERMS

SAFE FOR FREQUENT USE

8 FL OZ (236mL)

Miracle Brands, LLC

8924 E Pinnacle Peak Road

Suite G5 #519

Scottsdale, AZ 85255

www.MiracleBrandsUSA.com

Toll Free: (877) 753-0506

INGREDIENTS AND APPEARANCE

MIRACLE BRANDS HAND SANITIZER 
alcohol free hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69578-432
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
ALLANTOIN (UNII: 344S277G0Z)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
2,2'-((2-(DODECYLOXY)ETHYL)IMINO)BISETHANOL (UNII: 5MYL465X9V)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69578-432-08	236 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

Labeler - Global Health Solutions DBA Turn Therapeutics (079695890)

Registrant - Global Health Solutions DBA Turn Therapeutics (079695890)

Establishment
Name	Address	ID/FEI	Business Operations
Global Health Solutions DBA Turn Therapeutics		079695890	manufacture(69578-432)