Label: LOTRIMIN ANTIFUNGAL- miconazole nitrate aerosol, powder
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Contains inactivated NDC Code(s)
NDC Code(s): 11523-4140-2 - Packager: Bayer Healthcare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 6, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Flammable: Do not use while smoking or near heat or flame
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Directions
- wash affected area and dry thoroughly
- shake can well and spray 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
- in case of clogging, clean nozzle with a pin
- Other information
- Inactive ingredients
- Questions?
- Distribution
- PRINCIPAL DISPLAY PANEL - 133 g Can Label
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INGREDIENTS AND APPEARANCE
LOTRIMIN ANTIFUNGAL
miconazole nitrate aerosol, powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11523-4140 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength TALC (UNII: 7SEV7J4R1U) ISOBUTANE (UNII: BXR49TP611) Product Characteristics Color white (White to off-white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11523-4140-2 133 g in 1 CAN; Type 0: Not a Combination Product 09/01/1993 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 09/01/1993 Labeler - Bayer Healthcare LLC. (112117283)

