NDC 70859-053 Pedizolpak
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 70859-053?
What are the uses for Pedizolpak?
Which are Pedizolpak UNII Codes?
The UNII codes for the active ingredients in this product are:
- KETOCONAZOLE (UNII: R9400W927I)
- KETOCONAZOLE (UNII: R9400W927I) (Active Moiety)
- MICONAZOLE NITRATE (UNII: VW4H1CYW1K)
- MICONAZOLE (UNII: 7NNO0D7S5M) (Active Moiety)
Which are Pedizolpak 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:
- WATER (UNII: 059QF0KO0R)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ACETIC ACID (UNII: Q40Q9N063P)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LAURETH-4 (UNII: 6HQ855798J)
What is the NDC to RxNorm Crosswalk for Pedizolpak?
- RxCUI: 203088 - ketoconazole 2 % Topical Cream
- RxCUI: 203088 - ketoconazole 20 MG/ML Topical Cream
- RxCUI: 998525 - miconazole nitrate 2 % Topical Solution
- RxCUI: 998525 - miconazole nitrate 20 MG/ML Topical Solution
- RxCUI: 998526 - Fungoid 2 % tincture treatment kit
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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".