Label: BOA VIDA ANTIFUNGAL- miconazole nitrate cream
- NDC Code(s): 62654-147-01
- Packager: Central Solutions Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 18, 2018
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
Cleanse the affected area and dry thoroughly.
Apply a thin layer of product over affected area twice daily (morning and night), or as directed by a physician. Supervise children in the use of this product.
Athlete's foot
Pay special attention to the spaces between toes
wear well-fitting, ventilated shoes and change shoes and socks at least once daily
Athlete's foot and ringworm
use daily for 4 weeks
Jock Itch
use daily for 2 weeks. If condition persists longer, consult a doctor.
This product is not effective on scalp or nails.
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Cetearyl Alcohol, Cyclopentasiloxane, DMDM Hydantoin, Iodopropynyl Butylcarbamate, Glycerin, Glyceryl Stearate, PEG 100 Stearate, Isopropyl Palmitate, Polyquaternium-37, Propylene Glycol Dicaprylate Dicaprate, PPG-1 Trideceth-6, Propylene Glycol, Purified Water, Triethanolamine
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BOA VIDA ANTIFUNGAL
miconazole nitrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62654-147 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 2 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DMDM HYDANTOIN (UNII: BYR0546TOW) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) POLYQUATERNIUM-37 (10000 MPA.S) (UNII: 41QWS48DFN) PROPYLENE GLYCOL DICAPRYLATE (UNII: 581437HWX2) PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: O4446S9CRA) PPG-1 TRIDECETH-6 (UNII: 1K7417JX6Q) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62654-147-01 113 g in 1 TUBE; Type 0: Not a Combination Product 09/10/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 09/10/2018 Labeler - Central Solutions Inc (007118524) Establishment Name Address ID/FEI Business Operations Central Solutions Inc 007118524 manufacture(62654-147)