FDA Label for Conazol
View Indications, Usage & Precautions
Conazol Product Label
The following document was submitted to the FDA by the labeler of this product Laboratorios Liomont, S.a. De C.v.. 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
Miconazole nitrate 2%
Purpose
Antifungal
Uses
- effective in the treatment of most athlete's foot, jock itch and ringworm
- relieves itching, cracking, burning and discomfort associated with these conditions
Warnings
For external use only
Do Not Use
on children less than 2 years of age unless directed by a doctor
When Using This Product
• avoid contact with the eyes
Stop Use And Ask A Doctor If
- irritation occurs
- there is no improvement of athlete's foot or ringworm within 4 weeks or jock itch within 2 weeks
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- wash the affected area and dry thoroughly
- apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
- supervise children in the use of this product
- for athlete's foot, pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes,and change shoes
- for the athlete's foot and ringworm, use daily for 4 weeks
- for jock itch, use daily for 2 weeks
- not effective on the scalp or nails
and socks at least once daily
Other Information
- store at 20° to 25°C (68° to 77°F)
Inactive Ingredients
butylated hydroxyanisole, caprylic/capic triglyceride,carbomer 980, emulsifying wax, glycerin, methylparaben, propylene glycol, propylparaben, purified water, triethanolamine
Package Label
* Please review the disclaimer below.
