Laser Rejuvenation

Manufacturer
Universal Cosmetic Co., Ltd
Effective date
2010-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:34

Label at a glance#

ProductLaser Rejuvenation restoring damage skin
Active ingredientADENOSINE, ACETYL HEXAPEPTIDE-3, CENTELLA ASIATICA
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Adenosine, Copper Tripeptide, Acetyl Hexapeptide, Centella Asiatica Extract

OTC - PURPOSE SECTION

Uses
■ Helps to restore damaged skin after high or low power laser treatment including fraxel and IPL etc and medical treatment such as MTS and peeling.
■ Helps to repair aging skin including wrinkles and decrease in elasticity etc.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warning
For external use only
When using this product
■ Avoid contact with eyes. If contacts with eyes, rinse thoroughly with water.
■ If irritation occurs, discontinue use. If irritation persists, see a doctor.
Keep out of reach of the children

INDICATIONS & USAGE SECTION

Direction
■ Apply after cleansing.
■ Apply appropriate amounts onto the skin defect and damaged areas and then absorb patting gently, morning and night.

WARNINGS SECTION

Warning
For external use only
When using this product
■ Avoid contact with eyes. If contacts with eyes, rinse thoroughly with water.
■ If irritation occurs, discontinue use. If irritation persists, see a doctor.
Keep out of reach of the children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ADENOSINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52554-5001-12019-10-21C16284748780-1956f9ecf-cbcd-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52554-5001-1Laser Rejuvenationrestoring damage skin30 mL in 1 BOTTLE, PLASTICCREAM301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52554-5001LASER REJUVENATION RESTORING DAMAGE SKIN (ADENOSINE) CREAM [UNIVERSAL COSMETIC CO., LTD]1Legacy NDC, 1 package rows20100819_da884734-c4fc-479f-887e-e55ba6c8571e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACETYL HEXAPEPTIDE-3ACTIVE INGREDIENTL4EL31FWIL1
ADENOSINEACTIVE INGREDIENTK72T3FS5671
CENTELLA ASIATICAACTIVE INGREDIENT7M867G6T1U1
ACETYL HEXAPEPTIDE-3ACTIVE MOIETYL4EL31FWIL1
ADENOSINEACTIVE MOIETYK72T3FS5671
CENTELLA ASIATICAACTIVE MOIETY7M867G6T1U1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52554-500152554-5001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

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
ec0c2126-a7fa-448e-8805-21b2da0de858da884734-c4fc-479f-887e-e55ba6c8571e2010-08-19WarningsExact identifier
spl id: ec0c2126-a7fa-448e-8805-21b2da0de858
spl set id: da884734-c4fc-479f-887e-e55ba6c8571e

Reported adverse events (FAERS/openFDA)#

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