NDC 54860-402 Wellcare Sunstick 01
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 54860-402?
What are the uses for Wellcare Sunstick 01?
Which are Wellcare Sunstick 01 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Wellcare Sunstick 01 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:
- VANILLIN (UNII: CHI530446X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ETHYL VANILLIN (UNII: YC9ST449YJ)
- 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA)
- STEVIOSIDE (UNII: 0YON5MXJ9P)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- COCONUT OIL (UNII: Q9L0O73W7L)
- POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
* 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".