NDC 41520-693 Anti-aging Vitamin Complex 7-in-1 Broad Spectrum Spf15 Sunscreen
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Product Details
What is NDC 41520-693?
What are the uses for Anti-aging Vitamin Complex 7-in-1 Broad Spectrum Spf15 Sunscreen?
Which are Anti-aging Vitamin Complex 7-in-1 Broad Spectrum Spf15 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Anti-aging Vitamin Complex 7-in-1 Broad Spectrum Spf15 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PANTHENOL (UNII: WV9CM0O67Z)
- DOCOSANOL (UNII: 9G1OE216XY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- MAGNESIUM ASPARTATE (UNII: R17X820ROL)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- COPPER GLUCONATE (UNII: RV823G6G67)
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
- DIHYDROXYACETONE (UNII: O10DDW6JOO)
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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".