FDA Label for Blooskim Anti Dandruff
View Indications, Usage & Precautions
Blooskim Anti Dandruff Product Label
The following document was submitted to the FDA by the labeler of this product Good Manager Holdings Inc. 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.
Otc - Active Ingredient
ketoconazole 1%
Otc - Purpose
ANTI-DANDRUFF SHAMPOO
Indications & Usage
Controls flaking, scaling, and itching caused by dandruff
Otc - When Using
When using this product
Avoid contact with eyes
If contact occurs, rinse thoroughly with water.
Warnings
For external use only
Otc - Do Not Use
Do not use
On scalp that is broken or inflamed
If you are allergic to ingredients in this product
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Otc - Stop Use
Stop use and ask a doctor if
A rash appears.
Condition worsens or does not improve within 2-4 weeks.
If pregnant or breast-feeding, consult a doctor before use.
Dosage & Administration
Directions
adults and children 12 years and over
Wet hair thoroughly.
Apply shampoo, lather generously, and rinse thoroughly.
Repeat if necessary.
Use every 3-4 days for up to 8 weeks or as directed by a doctor.
Afterward, use as needed to control dandruff.
children under 12 years
Ask a doctor
Other Safety Information
Store at 20°C to 25°C (68°F to 77°F)
Inactive Ingredient
Citric Acid, Herba Violae, Euphorbia Hirta, Murraya Paniculata , Mentha Canadensis, Sophora Flavescens, Dittany Bark, Glabrous Greenbrier Rhizome, Mosla Cavaleriei Levl, Stellera Chamaejasme, Huang Bai, Sessile Stemona Root, Gleditsia Sinensis, Common Cnidium Fruit, Fructus Kochiae, Tea Tree Oil, Water
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