NDC 71521-395 Diabetic Foot Cream Professional
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What is NDC 71521-395?
What are the uses for Diabetic Foot Cream Professional?
Which are Diabetic Foot Cream Professional UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Diabetic Foot Cream Professional 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:
- LAURYL LAURATE (UNII: GPW77G0937)
- GLYCERIN (UNII: PDC6A3C0OX)
- CASTOR OIL (UNII: D5340Y2I9G)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- CITRAL (UNII: T7EU0O9VPP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- PROPANEDIOL (UNII: 5965N8W85T)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DITTRICHIA VISCOSA WHOLE (UNII: 3SYW69FH88)
- DOCOSANOL (UNII: 9G1OE216XY)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CANDELILLA WAX (UNII: WL0328HX19)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ORANGE OIL (UNII: AKN3KSD11B)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
What is the NDC to RxNorm Crosswalk for Diabetic Foot Cream Professional?
- RxCUI: 200010 - dimethicone 1 % Topical Cream
- RxCUI: 200010 - dimethicone 10 MG/ML Topical Cream
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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".