NDC 58443-0295 Traci Lynn Skin Iluminator Broad Spectrum Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises
- 58443-0295 - Traci Lynn Skin
Product Characteristics
Product Packages
NDC Code 58443-0295-3
Package Description: 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 58443-0295?
What are the uses for Traci Lynn Skin Iluminator Broad Spectrum Spf 50?
Which are Traci Lynn Skin Iluminator Broad Spectrum Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Traci Lynn Skin Iluminator Broad Spectrum Spf 50 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:
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- OXT-101 (UNII: 622325VBYO)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- NIACINAMIDE (UNII: 25X51I8RD4)
- OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
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[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".