FDA Label for Shailee Psoriasis Treatment
View Indications, Usage & Precautions
Shailee Psoriasis Treatment Product Label
The following document was submitted to the FDA by the labeler of this product Foshan Sugar Max Cosmetics Co.,ltd. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient Purpose
Salicylic Acid 3% Psoriasis and Dandruff Seborrheic Dermatitis
Uses
Controls flaking, scaling, and itching associated with dandruff.
Warnings
For external use only
Do not use
- On a damaged or inflamed scalp.
- If you are allergic to ingredients in this product.
- Avoid contact with the eyes.
- If contact occurs, rinse the eyes thoroughly with water.
- Rash appears.
- condition worsens or does not improve in 2-4 weeks.
When using this product
Stop use and ask a doctor if
If pregnant or breast-feeding, ask a doctor before use.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
| Adults and children aged 12 and over. |
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| Children under 12 years old. |
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Other Information
- store between 20° – 25°C (68° – 77°F)
- See bottom panel for lot number and expiration date
Inactive Ingredients
Purified Water, Sodium C-4-16 Olefin Sulfonate, Cocamidopropyl Betaine, PEG-120 Methyl Glucose Dioleate, Polyquaternium-7, Trolamine, Phospholipid EFA, DL Panthenol USP Powder, Vitamin E Acetate, Biotin, Hydrolyzed Keratin, Oxidized Keratin, Rosemary Oil, Tea Tree Oil, Peppermint Oil,Green Tea Extract, Ascorbic Acid, Manuka Honey
Product Label
* Please review the disclaimer below.
