NDC 61722-211 Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf33 Chocolate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61722 - Kosan Kozmetik Sanayi Ve Ticaret A.s.
- 61722-211 - Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf33 Chocolate
Product Packages
NDC Code 61722-211-00
Package Description: 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE
Product Details
What is NDC 61722-211?
What are the uses for Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf33 Chocolate?
Which are Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf33 Chocolate UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf33 Chocolate 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)
- PROPANEDIOL (UNII: 5965N8W85T)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- UREA (UNII: 8W8T17847W)
- ANOGEISSUS LEIOCARPUS BARK (UNII: U5TP1X38RH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LAURETH-12 (UNII: OAH19558U1)
- TREHALOSE (UNII: B8WCK70T7I)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- COTTON SEED (UNII: DI0ZRJ0MXN)
- FLAX SEED (UNII: 4110YT348C)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* Please review the disclaimer below.
[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".