MIRACLE AQUA PEELING- hyaluronate sodium gel

Miracle Aqua Peeling by

Drug Labeling and Warnings

Miracle Aqua Peeling 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

Apply a generous amount on face and gently massage.
Rinse thoroughly.

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, 1,2-Hexanediol, Alcohol, Arginine, Butylene Glycol, Camellia Sinensis Leaf Extract, Canavalia Gladiata Seed Extract, Carbomer, Caviar Extract, Cellulose, Centella Asiatica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ethylhexylglycerin, Fragrance, Glycyrrhiza Glabra (Licorice) Root Extract, Nasturtium Offcinale Extract, PEG-400, PEG-60 Hydrogenated Castor Oil , Polygonum Cuspidatum Root Extract, Rosmarinus Officinalis (Rosemary) Leaf Exreact, Scutellaria Baicalensis Root Extract, Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MIRACLE AQUA PEELING 
hyaluronate sodium gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72557-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	0.005 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ALCOHOL (UNII: 3K9958V90M)
ARGININE (UNII: 94ZLA3W45F)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72557-001-01	100 g in 1 CONTAINER; Type 0: Not a Combination Product	09/19/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/19/2018

Labeler - TOAS Co., Ltd. (694485346)

Registrant - TOAS Co., Ltd. (694485346)

Establishment
Name	Address	ID/FEI	Business Operations
TOAS Co., Ltd.		694485346	manufacture(72557-001)