NDC 71521-391 Diabetic Antifungal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71521 - Lavior Inc
- 71521-391 - Diabetic Antifungal
Product Packages
NDC Code 71521-391-50
Package Description: 50 g in 1 BOTTLE, PUMP
Product Details
What is NDC 71521-391?
What are the uses for Diabetic Antifungal?
Which are Diabetic Antifungal UNII Codes?
The UNII codes for the active ingredients in this product are:
- UNDECYLENIC ACID (UNII: K3D86KJ24N)
- UNDECYLENIC ACID (UNII: K3D86KJ24N) (Active Moiety)
Which are Diabetic Antifungal 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:
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- PROPANEDIOL (UNII: 5965N8W85T)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- STARCH, CORN (UNII: O8232NY3SJ)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- UREA (UNII: 8W8T17847W)
- CANDELILLA WAX (UNII: WL0328HX19)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DOCOSANOL (UNII: 9G1OE216XY)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DITTRICHIA VISCOSA WHOLE (UNII: 3SYW69FH88)
- SHEA BUTTER (UNII: K49155WL9Y)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PALMITIC ACID (UNII: 2V16EO95H1)
- TEA TREE OIL (UNII: VIF565UC2G)
- HYDROXYPROPYL BISPALMITAMIDE MONOETHANOLAMIDE (UNII: EVX7NC9YVE)
- ISOMERIZED SAFFLOWER ACID (UNII: 70S2158RCI)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
* Please review the disclaimer below.
[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".