FDA.reportPublic FDA data

XR CELLULAR MAGIC

Manufacturer
MESO SYSTEM S.A.
Effective date
2016-12-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:17

Label at a glance#

ProductXR CELLULAR MAGIC
Active ingredientHYALURONATE SODIUM
Label structure10 sections

Indications and 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

Dosage and administration

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

Label contents#

Full prescribing information#

Warnings

OTC - ASK DOCTOR SECTION

Stop use and ask a Doctor if skin rash occurs

WARNINGS

WARNINGS SECTION

  • 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

OTC - PURPOSE SECTION

  • 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

QUESTIONS OR COMMENTS ?

OTC - QUESTIONS SECTION

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

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

ProductProduct

INDICATIONS & USAGE SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

XR CELLULAR MAGIC

SKIN PROTECTANT

BoxBox

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70663-008-022020-01-31C16284748780-19d75b9d0-7054-f424-e053-dadaa90a57ceXR CELLULAR MAGIC

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70663-008-01XR CELLULAR MAGIC50 mL in 1 BOTTLEGEL501
70663-008-02XR CELLULAR MAGIC1 in 1 BOXGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70663-008XR CELLULAR MAGIC (SODIUM HYALURONATE) GEL [MESO SYSTEM S.A.]1Legacy NDC, 2 package rows20161229_43e51c3c-add2-3f98-e054-00144ff88e88.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70663-00870663-008-01, 70663-008-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYOXYL 35 CASTOR OIL6D4M1DAL6OIACT
BORAGO OFFICINALIS FLOWER7X23S1OW1NIACT
ASCORBYL PALMITATEQN83US2B0NIACT
DIPROPYLENE GLYCOLE107L85C40IACT
SODIUM MANNURONATE METHYLSILANOL6ZK10JO456IACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PEG-30 GLYCERYL LINOLEATEUPJ8VI2ZOCIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERYL ARACHIDONATEI4WS2B978BIACT
GLYCERYL LINOLENATESGB6X4G86KIACT
DEANOL2N6K9DRA24IACT
HYALURONATE SODIUMYSE9PPT4THACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
43e51c3c-add3-3f98-e054-00144ff88e8843e51c3c-add2-3f98-e054-00144ff88e882016-12-17WarningsExact identifier
spl id: 43e51c3c-add3-3f98-e054-00144ff88e88
spl set id: 43e51c3c-add2-3f98-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.