NDC 12961-113 Farewell Collection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12961 - Brisas Del Caribe Corp.
- 12961-113 - Farewell Collection
Product Packages
NDC Code 12961-113-11
Package Description: 53 mL in 1 TUBE
Product Details
What is NDC 12961-113?
What are the uses for Farewell Collection?
Which are Farewell Collection UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Farewell Collection 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- LAURETH-7 (UNII: Z95S6G8201)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- NIACINAMIDE (UNII: 25X51I8RD4)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SHEA BUTTER (UNII: K49155WL9Y)
- PEG-100 STEARATE (UNII: YD01N1999R)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".