NDC 58411-416 Revive Fermitif Neck Renewal Broad Spectrum Spf 15 Sunscreen
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What is NDC 58411-416?
What are the uses for Revive Fermitif Neck Renewal Broad Spectrum Spf 15 Sunscreen?
Which are Revive Fermitif Neck Renewal Broad Spectrum Spf 15 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (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 Revive Fermitif Neck Renewal Broad Spectrum Spf 15 Sunscreen 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)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SQUALANE (UNII: GW89575KF9)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- NEPIDERMIN (UNII: TZK30RF92W)
- BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TERMINALIA CATAPPA LEAF (UNII: 4XBZ9J585L)
- LEVOMENOL (UNII: 24WE03BX2T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- PYRROLIDONE CARBOXYLIC ACID (UNII: 6VT1YZM21H)
- ALLANTOIN (UNII: 344S277G0Z)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- TANNIC ACID (UNII: 28F9E0DJY6)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GERANIOL (UNII: L837108USY)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
* 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".