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Lustra Generic Name & Formulations
Legal Class
Rx
General Description
Hydroquinone 4%; crm; contains sulfites.
Pharmacological Class
Depigmenting agent.
See Also
How Supplied
Crm—1oz, 2oz
Manufacturer
Lustra Indications
Indications
UV-induced skin dyschromia and discoloration due to hormonal changes or skin trauma.
Lustra Dosage and Administration
Adult
Apply to affected areas twice daily. Discontinue if lightening effect does not occur after 2 months.
Children
Not recommended.
Lustra Contraindications
Not Applicable
Lustra Boxed Warnings
Not Applicable
Lustra Warnings/Precautions
Warnings/Precautions
Do skin sensitivity test before use; do not use if itching, vesicle formation or excessive inflammation occurs. Avoid sun and UV light. Not for use as a sunscreen. Avoid eyes. Pregnancy (Cat.C). Nursing mothers.
Lustra Pharmacokinetics
See Literature
Lustra Interactions
Not Applicable
Lustra Adverse Reactions
Adverse Reactions
Contact dermatitis.
Lustra Clinical Trials
See Literature
Lustra Note
Not Applicable
Lustra Patient Counseling
See Literature
