Pure Porcelain Skin Defense Makeup Spf 15 Jafra
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Questions & Answers
Side Effects & Adverse Reactions
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Manufacturer Warnings
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FDA Labeling Changes
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Uses
Azelaic Acid Gel, 15% is indicated for topical treatment of the inflammatory papules and pustules of mild to moderate rosacea. Although some reduction of erythema which was present in patients with papules and pustules of rosacea occurred in clinical studies, efficacy for treatment of erythema in rosacea in the absence of papules and pustules has not been evaluated.
History
There is currently no drug history available for this drug.
Other Information
Azelaic Acid (azelaic acid) Gel, 15%, is an aqueous gel which contains azelaic acid, a naturally-occurring saturated dicarboxylic acid. Chemically, azelaic acid is 1,7-heptanedicarboxylic acid. The molecular formula for azelaic acid is C9 H16 O4. It has the following structure:
Azelaic acid has a molecular weight of 188.22. It is a white, odorless crystalline solid. It is poorly soluble in water at 20°C (0.24%) but freely soluble in boiling water and in ethanol.
Azelaic AcidGelis a white to yellowish white opaque gel for topical use; each gram contains 0.15 gm azelaic acid (15%w/w) in an aqueous gel base containing benzoic acid (as a preservative), disodium EDTA, lecithin, medium-chain triglycerides, polyacrylic acid, polysorbate 80, propylene glycol, purified water, and sodium hydroxide to adjust pH.
Sources
Pure Porcelain Skin Defense Makeup Spf 15 Jafra Manufacturers
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Jafra Cosmetics International Inc
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Pure Porcelain Skin Defense Makeup Spf 15 Jafra | Alvogen, Inc.
• Apply and gently massage a thin layer of Azelaic Acid Gel into the affected areas on the face twice daily (morning and evening). • Use only very mild soaps or soapless cleansing lotion before application of Azelaic Acid Gel. • Cosmetics may be applied after the application of Azelaic Acid Gel has dried. • Avoid the use of occlusive dressings or wrappings. • Instruct patients to avoid spicy foods, thermally hot foods and drinks, alcoholic beverages. • Patients should be reassessed if no improvement is observed upon completing 12 weeks of therapy. • Not for oral, ophthalmic or intravaginal use.
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