NDC 76458-201 Light Day Sunscreen Broad Spectrum Spf 37
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76458 - Circadia By Dr Pugliese, Inc.
- 76458-201 - Light Day Sunscreen Broad Spectrum Spf 37
Product Packages
NDC Code 76458-201-02
Package Description: 59 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 76458-201?
What are the uses for Light Day Sunscreen Broad Spectrum Spf 37?
Which are Light Day Sunscreen Broad Spectrum Spf 37 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)
Which are Light Day Sunscreen Broad Spectrum Spf 37 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ISOMALT (UNII: S870P55O2W)
- APRICOT (UNII: 269CJD5GZ9)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ANIBA ROSAEODORA WOOD (UNII: NE01NKA8B2)
- LIME PEEL (UNII: 544EQK5Q0W)
- ORANGE PEEL (UNII: TI9T76XD44)
- VANILLA (UNII: Q74T35078H)
- CITRUS MAXIMA FRUIT RIND (UNII: 5NX3G75CA6)
- COCONUT OIL (UNII: Q9L0O73W7L)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- WINE GRAPE (UNII: 3GOV20705G)
* 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".