MIRACLE LASER MASK- hyaluronate sodium cream

Miracle Laser Mask by

Drug Labeling and Warnings

Miracle Laser Mask by is a Otc medication manufactured, distributed, or labeled by TOAS Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium Hyaluronate 0.005%

PURPOSE

Moisturizing

INDICATIONS & USAGE

Helps to keep skin moistness

DOSAGE & ADMINISTRATION

Remove film and apply mask over cleansed face. Leave on for 15-30 minutes then remove.

WARNINGS

For external use only.
Do not use on damaged or broken skin.
When using this product, keep out of eyes. Rinse with water to remove.
Stop using and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT

Water, Glycerin, Butylene Glycol, Propylene Glycol, Aloe Barbadensis Leaf Extract, Portulaca Oleracea Extract, Arginine, Carbomer, Polysorbate 80, Betaine, Allantoin, Methylparaben, Hydrolyzed Collagen, Sodium PCA, Disodium EDTA, Dipotassium Glycyrrhizate, Hamamelis Virginiana (Witchhazel) Water, Tocopheryl Acetate, Sodium Polyacrylate, Fragrance, Propylparaben, OligoPepTide-1

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MIRACLE LASER MASK 
hyaluronate sodium cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72557-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	0.0014 g  in 28 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARGININE (UNII: 94ZLA3W45F)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
BETAINE (UNII: 3SCV180C9W)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72557-005-02	10 in 1 CARTON	09/24/2018
1	NDC: 72557-005-01	28 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/24/2018

Labeler - TOAS Co., Ltd. (694485346)

Registrant - TOAS Co., Ltd. (694485346)

Establishment
Name	Address	ID/FEI	Business Operations
TOAS Co., Ltd.		694485346	manufacture(72557-005)