Label: NEKVNRO CLOTRIMAZOLE- clotrimazole1%, miconazole1%clotrimazole ointment
- NDC Code(s): 84010-030-01, 84010-030-02, 84010-030-03, 84010-030-04
- Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 13, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
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Directions
·adults and children 12 years and older:
● use the tip of the cap to break the seal and open the tube
●wash the affected skin with soap and water and dry completely before applying
● for athlete's foot between the toes:apply to affected skin between and around the toes twice a day for 1 week(morning and night), or once a day for 4 weeks, or as directed by a doctor. Wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.
●for jock itch and ringworm: apply once a day to affected skin for 2 weeks or as directed by a doctor●wash hands after each use
●children under 12 years: aska doctor
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NEKVNRO CLOTRIMAZOLE
clotrimazole1%, miconazole1%clotrimazole ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84010-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE (UNII: 7NNO0D7S5M) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE 1 g in 100 g CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE 1 g in 100 g Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) PEPPERMINT (UNII: V95R5KMY2B) TROLAMINE (UNII: 9O3K93S3TK) DIMETHICONE (UNII: 92RU3N3Y1O) GENTIANA MANSHURICA ROOT (UNII: C1F2NZ8U3L) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84010-030-01 20 g in 1 TUBE; Type 0: Not a Combination Product 09/13/2024 2 NDC:84010-030-02 30 g in 1 TUBE; Type 0: Not a Combination Product 09/13/2024 3 NDC:84010-030-03 42.5 g in 1 TUBE; Type 0: Not a Combination Product 09/13/2024 4 NDC:84010-030-04 50 g in 1 TUBE; Type 0: Not a Combination Product 09/13/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 09/13/2024 Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056) Establishment Name Address ID/FEI Business Operations Jiangxi Hemei Pharmaceutical Co., Ltd 724892056 manufacture(84010-030)