NDC 0363-5203 Miconazole 3 Walgreen Company
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 0363-5203?
What are the uses for Miconazole 3 Walgreen Company?
Which are Miconazole 3 Walgreen Company UNII Codes?
The UNII codes for the active ingredients in this product are:
- MICONAZOLE NITRATE (UNII: VW4H1CYW1K)
- MICONAZOLE (UNII: 7NNO0D7S5M) (Active Moiety)
Which are Miconazole 3 Walgreen Company Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN (UNII: 2G86QN327L)
- 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)
What is the NDC to RxNorm Crosswalk for Miconazole 3 Walgreen Company?
- RxCUI: 992765 - miconazole nitrate 200 MG Vaginal Insert
- RxCUI: 992766 - {1 (9000 MG) (miconazole nitrate 20 MG/ML Vaginal Cream) / 3 (miconazole nitrate 200 MG Vaginal Insert) } Pack
- RxCUI: 992766 - miconazole nitrate 200 MG Vaginal Insert (3) / miconazole nitrate 2 % Vaginal Cream (9 GM) Pack
- RxCUI: 992766 - miconazole 3 Day (3 - 200 MG miconazole nitrate vaginal insert / 9 GM miconazole nitrate 2 % topical vaginal cream)
- RxCUI: 992766 - miconazole 3 Day Vaginal Insert Combination Pack
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Patient Education
Miconazole Vaginal
Vaginal miconazole is used to treat vaginal yeast infections in adults and children 12 years of age and older. Miconazole is in a class of antifungal medications called imidazoles. It works by stopping the growth of fungi that cause infection.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".