FDA Label for Lotrimin Af Jock Itch
View Indications, Usage & Precautions
Lotrimin Af Jock Itch Product Label
The following document was submitted to the FDA by the labeler of this product Bayer Healthcare Llc.. 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.
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Drug Facts
Active Ingredient
Miconazole nitrate 2%
Purpose
Antifungal
Uses
- Cures most jock itch (tinea cruris)
- relieves Itching, burning, scaling, discomfort, and chafing associated with jock itch
Warnings
For external use only
Do not use on children under 2 years of age unless directed by a doctor.
When Using This Product
avoid contact with the eyes
Otc - Stop Use
Stop use and ask a doctor if
- irritation occurs
- if there is no improvement within 2 weeks
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- wash affected area and dry thoroughly
- sprinkle a thin layer over affected area twice daily (morning and night)
- supervise children in the use of this product
- use daily for 2 weeks
- if condition persists longer, ask a doctor
- this product is not effective on the scalp or nails
Other Information
store between 20° to 25°C (68° to 77°F)
Inactive Ingredients
benzethonium chloride, corn starch, kaolin, sodium bicarbonate, zinc oxide
Pdp
LOTRIMIN ® AF
miconazole nitrate
ANTIFUNGAL
MEDICATED POWDER
JOCK ITCH
CLINICALLY PROVEN
to cure most
jock itch
RELIEVES
- Itching
- Burning
- Scaling
- Chafing
NET WT 177g (6.25 OZ)
* Please review the disclaimer below.