NDC 43447-4410 Skin Sake Surface Protectant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43447 - Skin Sake, Llc
- 43447-4410 - Skin Sake Surface Protectant
Product Packages
NDC Code 43447-4410-0
Package Description: 113.6 g in 1 TUBE
NDC Code 43447-4410-2
Package Description: 100 PACKET in 1 BOX / 8 g in 1 PACKET (43447-4410-1)
Product Details
What is NDC 43447-4410?
What are the uses for Skin Sake Surface Protectant?
Which are Skin Sake Surface Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Skin Sake Surface Protectant 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)
- BORIC ACID (UNII: R57ZHV85D4)
- CASTOR OIL (UNII: D5340Y2I9G)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- COD LIVER OIL (UNII: BBL281NWFG)
- D&C GREEN NO. 6 (UNII: 4QP5U84YF7)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- MINERAL OIL (UNII: T5L8T28FGP)
- BALSAM PERU (UNII: 8P5F881OCY)
- D&C RED NO. 17 (UNII: ND733RX3JN)
- VITAMIN A (UNII: 81G40H8B0T)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- PETROLATUM (UNII: 4T6H12BN9U)
- WHITE WAX (UNII: 7G1J5DA97F)
- D&C YELLOW NO. 11 (UNII: 44F3HYL954)
What is the NDC to RxNorm Crosswalk for Skin Sake Surface Protectant?
- RxCUI: 283411 - dimethicone 2 % Topical Ointment
- RxCUI: 283411 - dimethicone 0.02 MG/MG Topical Ointment
* 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".