NDC 68327-002 Natural Fx
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68327 - Cover Fx Skin Care, Inc.
- 68327-002 - Natural Fx
Product Packages
NDC Code 68327-002-01
Package Description: 30 mL in 1 TUBE
Product Details
What is NDC 68327-002?
What are the uses for Natural Fx?
Which are Natural Fx 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Natural Fx 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 (UNII: NMQ347994Z)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- NEOPENTYL GLYCOL DICAPRATE (UNII: 77T908SE82)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIACONTANYL PVP (WP-660) (UNII: N0SS3Q238D)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- HYDROGENATED POLYBUTENE (370 MW) (UNII: V5H8103878)
- CHOLESTERYL HYDROXYSTEARATE (UNII: O6K1LG6N4D)
- TOCOPHEROL (UNII: R0ZB2556P8)
- LEVOMENOL (UNII: 24WE03BX2T)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SORBIC ACID (UNII: X045WJ989B)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CHROMIC OXIDE (UNII: X5Z09SU859)
* 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".