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HSA Approval

Obagi Nu-Derm Blender

Approval Number

SIN13519P

Drug Name

Obagi Nu-Derm Blender

Product Name

Obagi Nu-Derm Blender

Approval Date

August 13, 2008

Registrant

NEOASIA (S) PTE LTD

Regulatory Information

Registrant

NEOASIA (S) PTE LTD

Drug Type

Therapeutic

Forensic Classification

Prescription Only

Formulation Information

Dosage Form

CREAM

Route of Administration

TOPICAL

Medical Information

ATC Code

D11AX11

ATC Item Name

hydroquinone

Manufacturer Information

Pharmaceutical Manufacturer

NEOASIA (S) PTE LTD

Manufacturers

Pure Tek Corporation

Active Ingredients

Ingredient Name

Hydroquinone

Strength

4%

Drug MonographHydroquinone

Documents

Package Inserts

Obagi Nu-Derm PI.pdf

Approved: July 25, 2022

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Obagi Nu-Derm Blender - HSA Approval | MedPath