NDC 61722-349 Flormar Cc 04 Anti Fatigue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61722 - Kosan Kozmetik Sanayi Ve Ticaret Anonim Sirketi
- 61722-349 - Flormar Cc 04 Anti Fatigue
Product Packages
NDC Code 61722-349-00
Package Description: 1 TUBE in 1 BOX / 35 mL in 1 TUBE
Product Details
What is NDC 61722-349?
What are the uses for Flormar Cc 04 Anti Fatigue?
Which are Flormar Cc 04 Anti Fatigue UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Flormar Cc 04 Anti Fatigue 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)
- BETAINE (UNII: 3SCV180C9W)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- PANTHENOL (UNII: WV9CM0O67Z)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- LAURETH-12 (UNII: OAH19558U1)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
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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".