NDC 69039-258 Sun Bum Mineral Spf 30 Tinted Sunscreen Face
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69039 - Sun Bum Llc
- 69039-258 - Sun Bum Mineral Spf 30 Tinted Sunscreen Face
Product Packages
NDC Code 69039-258-00
Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE
Product Details
What is NDC 69039-258?
What are the uses for Sun Bum Mineral Spf 30 Tinted Sunscreen Face?
Which are Sun Bum Mineral Spf 30 Tinted Sunscreen Face UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sun Bum Mineral Spf 30 Tinted Sunscreen Face 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)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- RICE BRAN (UNII: R60QEP13IC)
- ROSEMARY (UNII: IJ67X351P9)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- OCTYLDODECYL OLEATE (UNII: MCA43PK7MH)
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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".