NDC 42479-214 Footlogix Moisturizing Diabetic Formula
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Product Details
What is NDC 42479-214?
What are the uses for Footlogix Moisturizing Diabetic Formula?
Which are Footlogix Moisturizing Diabetic Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Footlogix Moisturizing Diabetic Formula 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POVIDONE (UNII: FZ989GH94E)
- SORBITOL (UNII: 506T60A25R)
- SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- UREA (UNII: 8W8T17847W)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Footlogix Moisturizing Diabetic Formula?
- RxCUI: 1302746 - dimethicone 1 % Topical Foam
- RxCUI: 1302746 - dimethicone 10 MG/ML Topical Foam
- RxCUI: 1302751 - footlogix Moisturizing Diabetic Formula 1 % Topical Foam
- RxCUI: 1302751 - dimethicone 10 MG/ML Topical Foam [Footlogix Moisturizing Diabetic Formula]
- RxCUI: 1302751 - Footlogix Moisturizing Diabetic Formula 1 % Topical Foam
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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".