NDC 58503-116 Diabetics Foot Cream 4 Oz
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58503 - China Ningbo Shangge Cosmetic Technology Corp
- 58503-116 - Diabetics Foot Cream
Product Packages
NDC Code 58503-116-01
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 58503-116?
What are the uses for Diabetics Foot Cream 4 Oz?
Which are Diabetics Foot Cream 4 Oz UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Diabetics Foot Cream 4 Oz 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:
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- C13-16 ISOPARAFFIN (UNII: LED42LZG6O)
- LAURETH-7 (UNII: Z95S6G8201)
- POLYQUATERNIUM-22 (4500 MPA.S) (UNII: H3W1D31JAR)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- PANTHENOL (UNII: WV9CM0O67Z)
- PEG-100 STEARATE (UNII: YD01N1999R)
- LAURETH-25 (UNII: RPD53041LR)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
What is the NDC to RxNorm Crosswalk for Diabetics Foot Cream 4 Oz?
- RxCUI: 631803 - dimethicone 1 % / petrolatum 30 % Topical Cream
- RxCUI: 631803 - dimethicone 10 MG/ML / petrolatum 300 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".