NDC 61722-290 Flormar Bb White Bw01 Light
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61722 - Kosan Kozmetik Sanayi Ve Ticaret A.s.
- 61722-290 - Flormar Bb White Bw01 Light
Product Packages
NDC Code 61722-290-00
Package Description: 1 TUBE in 1 BOX / 40 mL in 1 TUBE
Product Details
What is NDC 61722-290?
What are the uses for Flormar Bb White Bw01 Light?
Which are Flormar Bb White Bw01 Light 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)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Flormar Bb White Bw01 Light 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/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- LAURETH-12 (UNII: OAH19558U1)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
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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".