NDC 63730-216 Tensolift
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 63730-216?
What are the uses for Tensolift?
Which are Tensolift UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- 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 Tensolift 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)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALLANTOIN (UNII: 344S277G0Z)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- UREA (UNII: 8W8T17847W)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SERINE (UNII: 452VLY9402)
- SORBITOL (UNII: 506T60A25R)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- TROLAMINE (UNII: 9O3K93S3TK)
- LEVOMENOL (UNII: 24WE03BX2T)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERYL MONOOLEATE (UNII: 4PC054V79P)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- GERANIOL (UNII: L837108USY)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- LINALOOL, DL- (UNII: D81QY6I88E)
- CINNAMYL ALCOHOL (UNII: SS8YOP444F)
- CITRAL (UNII: T7EU0O9VPP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
* 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".