NDC 69549-003 Blurred Lines Cc Creme Broad Spectrum Spf 20 Shade 03 Medium/dark
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69549-003?
What are the uses for Blurred Lines Cc Creme Broad Spectrum Spf 20 Shade 03 Medium/dark?
Which are Blurred Lines Cc Creme Broad Spectrum Spf 20 Shade 03 Medium/dark UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Blurred Lines Cc Creme Broad Spectrum Spf 20 Shade 03 Medium/dark 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:
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LAUROYL LYSINE (UNII: 113171Q70B)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- GERANIOL (UNII: L837108USY)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- TALC (UNII: 7SEV7J4R1U)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".