Label: ALOE VESTA- miconazole nitrate ointment
- NDC Code(s): 53329-774-14, 53329-774-64
- Packager: Medline Industries, LP
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 2, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
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Uses
- cures most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis)
- relieves itching, scaling, cracking, burning, redness, soreness, irritation, and discomfort that accompany these conditions
- for the treatment of most superficial skin infections caused by yeast (Candida albicans)
- follow a physician's instructions when treating Candida albicans
- Warnings
-
Directions
- clean the affected area and dry thoroughly
- apply a thin layer of ointment over affected area twice daily (morning and night) or as directed by a physician
- supervise children in use of this product
- for athlete's foot: pay close attention to 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
- this product is not effective on the scalp or nails
- Inactive ingredients
- Manufacturing Information
- Package Label
-
INGREDIENTS AND APPEARANCE
ALOE VESTA
miconazole nitrate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53329-774 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) MINERAL OIL (UNII: T5L8T28FGP) BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T) WHITE PETROLATUM (UNII: B6E5W8RQJ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53329-774-14 56 g in 1 TUBE; Type 0: Not a Combination Product 09/30/2020 11/30/2025 2 NDC:53329-774-64 141 g in 1 TUBE; Type 0: Not a Combination Product 09/30/2020 11/30/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 09/30/2020 11/30/2025 Labeler - Medline Industries, LP (025460908) Registrant - Medline Industries, LP (025460908)