XR CELLULAR MAGIC- sodium hyaluronate gel

XR CELLULAR MAGIC by

Drug Labeling and Warnings

XR CELLULAR MAGIC by is a Otc medication manufactured, distributed, or labeled by MESO SYSTEM S.A.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Warnings

Stop use and ask a Doctor if skin rash occurs

WARNINGS

• For external use only
• Stop use and ask a doctor if skin rash occur.s
• Avoid the product from entering your eyes
• Children under 6 months Ask a Doctor

USES

• Helps to reduce facial expression lines caused by the excessive contraction of muscles envolved in this phenomenos and
• helps to slow the aging process caused by the repeated facil movements. Excellent revitalizing and regenerating properties that provides nutrient to the dermis

KEEP OUT OF REACH OF CHILDREN

• Keep out of the reach of chuldren.
• In case of overdose get medical help or Contact a Poison Control Center right away.

DIRECTIONS

• Apply a small amount in the face and neck, morning and evening

QUESTIONS OR COMMENTS ?

• +35 1227347125 M-F: 9:00 am to 5:00 pm

ACTIVE INGREDIENTS

Active Ingredients Purpose

Sodium Hyaluronate 0.1%....................................Skin Protectant

Inactive Ingredients

Water, Propylene Glycol, Methylsilanol Mannuronate, Glyceryl Linoleate, Glyceryl Linolenate, Glyceryl Arachidonate, Phenoxyethanol, Peg-35 Castor Oil, Borago Officinalis Extract, Ascorbyl Palmitate, Dimethyl Mea, Ethylhexylglycerin

INDICATIONS & USAGE

Apply a small amount in the face and neck, morning and evening

PRINCIPAL DISPLAY PANEL

XR CELLULAR MAGIC

SKIN PROTECTANT

INGREDIENTS AND APPEARANCE

XR CELLULAR MAGIC 
sodium hyaluronate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70663-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	0.1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POLYOXYL 35 CASTOR OIL (UNII: 6D4M1DAL6O)	0.2 mg  in 1 mL
BORAGO OFFICINALIS FLOWER (UNII: 7X23S1OW1N)	0.2 mg  in 1 mL
ASCORBYL PALMITATE (UNII: QN83US2B0N)	0.1 mg  in 1 mL
DIPROPYLENE GLYCOL (UNII: E107L85C40)	10 mg  in 1 mL
SODIUM MANNURONATE METHYLSILANOL (UNII: 6ZK10JO456)	5 mg  in 1 mL
WATER (UNII: 059QF0KO0R)	80.3 mg  in 1 mL
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.9 mg  in 1 mL
PEG-30 GLYCERYL LINOLEATE (UNII: UPJ8VI2ZOC)	1 mg  in 1 mL
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.1 mg  in 1 mL
GLYCERYL ARACHIDONATE (UNII: I4WS2B978B)	1 mg  in 1 mL
GLYCERYL LINOLENATE (UNII: SGB6X4G86K)	1 mg  in 1 mL
DEANOL (UNII: 2N6K9DRA24)	0.1 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70663-008-02	1 in 1 BOX	12/17/2016
1	NDC: 70663-008-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/17/2016

Labeler - MESO SYSTEM S.A. (768263100)

Registrant - MESO SYSTEM S.A. (768263100)

Establishment
Name	Address	ID/FEI	Business Operations
MESO SYSTEM S.A.		768263100	manufacture(70663-008)