NDC 63550-809 Sunbar Spf 48
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63550 - Kamins Dermatologics Inc.
- 63550-809 - Sunbar Spf 48
Product Packages
NDC Code 63550-809-10
Package Description: 120 mL in 1 BOX
Product Details
What is NDC 63550-809?
What are the uses for Sunbar Spf 48?
Which are Sunbar Spf 48 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sunbar Spf 48 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:
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ACER SACCHARUM SAP (UNII: 75UOH57984)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARETH-100 (UNII: 4OH5W9UM87)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- STEARETH-2 (UNII: V56DFE46J5)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
* 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".