NDC | 63736-019-03 |
Set ID | 910d81cd-67dc-4fdf-94cf-4eb3b1dca0fd |
Category | HUMAN OTC DRUG LABEL |
Packager | Insight Pharmaceuticals LLC |
Generic Name | |
Product Class | Azole Antifungal |
Product Number | |
Application Number | NDA020670 |
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
-
Warnings
For vaginal use only
Ask a doctor before use if you have
-
vaginal itching and discomfort for the first time
-
lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge. You may have a more serious condition.
- vaginal yeast infections often (such as once a month or 3 in 6 months). You could be pregnant or have a serious underlying medical cause for your symptoms, including diabetes, or a weakened immune system.
- been exposed to the human immunodeficiency virus (HIV) that causes AIDS
Ask a doctor or pharmacist before use if you are
taking the prescription blood thinning medicine warfarin, because bleeding or bruising may occur
When using this product
- do not use tampons, douches, spermicides or other vaginal products. Condoms and diaphragms may be damaged and fail to prevent pregnancy or sexually transmitted diseases (STDs)
- do not have vaginal intercourse
- mild increase in vaginal burning, itching or irritation may occur
- if you do not get complete relief ask a doctor before using another product.
-
vaginal itching and discomfort for the first time
-
Directions
- before using this product read the enclosed consumer information leaflet for complete directions and information
- adults and children 12 years of age and over:
▪ vaginal insert: with a disposable applicator, place the insert into the vagina at bedtime. Throw applicator away after use.
▪ external cream: squeeze a small amount of cream onto your fingertip. Apply the cream onto the itchy, irritated skin outside the vagina. Use 2 times daily for up to 7 days, as needed. - children under 12 years of age: ask a doctor.
- before using this product read the enclosed consumer information leaflet for complete directions and information
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MONISTAT 3 COMBINATION PACK 3 OVULE INSERTS
miconazole nitrate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-019 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63736-019-03 1 in 1 PACKAGE, COMBINATION; Type 0: Not a Combination Product 04/16/1996 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 KIT 3 Part 2 1 TUBE 9 g Part 1 of 2 MICONAZOLE NITRATE
miconazole nitrate suppositoryProduct Information Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Miconazole Nitrate (UNII: VW4H1CYW1K) (Miconazole - UNII:7NNO0D7S5M) Miconazole Nitrate 200 mg Inactive Ingredients Ingredient Name Strength Gelatin (UNII: 2G86QN327L) Glycerin (UNII: PDC6A3C0OX) Titanium Dioxide (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 3 in 1 KIT; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020670 04/16/1996 Part 2 of 2 MICONAZOLE NITRATE
miconazole nitrate creamProduct Information Route of Administration VAGINAL 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 Benzoic Acid (UNII: 8SKN0B0MIM) Cetyl Alcohol (UNII: 936JST6JCN) Isopropyl Myristate (UNII: 0RE8K4LNJS) Polysorbate 60 (UNII: CAL22UVI4M) Potassium Hydroxide (UNII: WZH3C48M4T) Propylene Glycol (UNII: 6DC9Q167V3) Water (UNII: 059QF0KO0R) Stearyl Alcohol (UNII: 2KR89I4H1Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 9 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 NDA NDA020670 04/16/1996 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020670 04/16/1996 Labeler - Insight Pharmaceuticals LLC (055665422)