NDC | 75940-121-02, 75940-121-30, 75940-121-46 |
Set ID | cbd28006-06d9-4e1c-96bb-40034e2b3649 |
Category | HUMAN OTC DRUG LABEL |
Packager | MarcasUSA LLC |
Generic Name | |
Product Class | Azole Antifungal |
Product Number | |
Application Number | PART333C |
- Active Ingredients Purpose
- INDICATIONS & USAGE
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
-
Directions
- wash the affected area and dry thoroughly
- apply 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 the athlete's foot and ringworm, use daily for 4 weeks
- for jock itch, use daily for 2 weeks
- not effective on the scalp or nails
- Other Information
- INACTIVE INGREDIENT
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Usos
- Precauciones
- No lo use
- Al utilizar este producto
- Pare su uso consulte al médico, si
- Mantener fuera del alcance de los niños.
-
Modo de Empleo
- limpie y seque bien el área afectada
- aplique una capa fina del producto sobre el área
afectada dos veces al diá (mañana y noche) o según
las indicaciones de un médico - supervise a los niños en el uso de este producto
- para el pie de atleta, poner especial atención a los espacios
entre los dedos de los pies, llevar zapatos ventilados y ajustados,
cambiar los calcetines y zapatos al menos una vez al dia - para el pie de atleta, usar diariamente por 4 semanas
- para tiña inguinal, usar diariamente por 2 semanas
- no es eficaz en el cuero cabelludo o las uñas
- Otra información
- INACTIVE INGREDIENT
- Ingredientes Inactivos
- SPL UNCLASSIFIED SECTION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 1.05 oz (30 g)
-
INGREDIENTS AND APPEARANCE
CONAZOL
miconazole nitrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75940-121 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 BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) TRICAPRIN (UNII: O1PB8EU98M) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75940-121-30 30 g in 1 TUBE; Type 0: Not a Combination Product 08/01/2014 2 NDC:75940-121-46 130 g in 1 CAN; Type 0: Not a Combination Product 08/01/2014 3 NDC:75940-121-02 2 g in 1 PACKET; Type 0: Not a Combination Product 08/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 08/01/2014 Labeler - MarcasUSA LLC (016139820) Registrant - MarcasUSA LLC (016139820) Establishment Name Address ID/FEI Business Operations Laboratorios Liomont, S.A. de C.V. 810347807 manufacture(75940-121)