NDC 61722-356 Flormar Mattifying Bb 01 Fair
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 61722-356?
What are the uses for Flormar Mattifying Bb 01 Fair?
Which are Flormar Mattifying Bb 01 Fair UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Flormar Mattifying Bb 01 Fair 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- 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)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
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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".