Label: CONAZOL- miconazole nitrate cream
- NDC Code(s): 59208-001-02, 59208-001-30
- Packager: Laboratorios Liomont, S.A. de C.V.
- Category: HUMAN OTC DRUG LABEL
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 January 31, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- 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 Ingredients
- Package Label
- Sample Package
-
INGREDIENTS AND APPEARANCE
CONAZOL
miconazole nitrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59208-001 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) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (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:59208-001-30 30 g in 1 TUBE; Type 0: Not a Combination Product 03/01/2019 2 NDC:59208-001-02 1 in 1 PACKAGE 05/01/2023 2 2 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M005 03/01/2019 Labeler - Laboratorios Liomont, S.A. de C.V. (810347807) Establishment Name Address ID/FEI Business Operations Laboratorios Liomont, S.A. de C.V. 810347807 manufacture(59208-001)