Label: TING- miconazole nitrate aerosol, powder
- NDC Code(s): 63736-532-05
- Packager: Insight Pharmaceuticals LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 6, 2023
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Warnings
For external use onlyFlammability Warning: Contents under pressure. Do not puncture or incinerate. Flammable mixture; do not use near fire or flame, or expose to heat or temperatures above 49°C (120°F). Use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
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Directions
▪ clean the affected area and dry thoroughly▪ shake can well, hold 4" to 6" from skin. Spray 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 and socks at least once daily.▪ for athlete's foot and ringworm use daily for 4 weeks; for jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor.
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INGREDIENTS AND APPEARANCE
TING
miconazole nitrate aerosol, powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-532 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 2.56 g in 128 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ALCOHOL (UNII: 3K9958V90M) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) STEARALKONIUM HECTORITE (UNII: OLX698AH5P) ISOBUTANE (UNII: BXR49TP611) BUTANE (UNII: 6LV4FOR43R) PROPANE (UNII: T75W9911L6) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63736-532-05 128 g in 1 CAN; Type 0: Not a Combination Product 07/16/2009 05/02/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 07/16/2009 05/02/2025 Labeler - Insight Pharmaceuticals LLC (055665422)