NDC 49817-1989 Fresh Sugar Plum Tinted Lip Treatment Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49817 - Guerlain
- 49817-1989 - Fresh Sugar Plum Tinted Lip Treatment Spf 15
Product Packages
NDC Code 49817-1989-4
Package Description: 1 CARTRIDGE in 1 CARTON / 4.3 g in 1 CARTRIDGE (49817-1989-9)
Product Details
What is NDC 49817-1989?
Which are Fresh Sugar Plum Tinted Lip Treatment Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Fresh Sugar Plum Tinted Lip Treatment Spf 15 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:
- WHITE WAX (UNII: 7G1J5DA97F)
- CASTOR OIL (UNII: D5340Y2I9G)
- JOJOBA OIL (UNII: 724GKU717M)
- 1-DECANOL (UNII: 89V4LX791F)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- RIBES NIGRUM SEED OIL (UNII: GKE1188837)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GLYCYRRHIZIN, AMMONIATED (UNII: 3VRD35U26C)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- VANILLIN (UNII: CHI530446X)
- PASSIFLORA INCARNATA SEED OIL (UNII: S0SU5AC95J)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- RICINOLEIC ACID (UNII: I2D0F69854)
* 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".