NDC 54235-204 Protectyl Soleil Moisturizing Sunscreen Lotion High Protection Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54235 - Yves Rocher North America Inc. Dba Laboratoire De Biologie Vegetal Yves Rocher
- 54235-204 - Protectyl Soleil Moisturizing Sunscreen Lotion High Protection Spf 30
Product Packages
NDC Code 54235-204-08
Package Description: 150 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54235-204?
What are the uses for Protectyl Soleil Moisturizing Sunscreen Lotion High Protection Spf 30?
Which are Protectyl Soleil Moisturizing Sunscreen Lotion High Protection Spf 30 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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Protectyl Soleil Moisturizing Sunscreen Lotion High Protection Spf 30 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:
- ACER SACCHARUM BARK/SAP (UNII: Z120VL0KAC)
- ALLANTOIN (UNII: 344S277G0Z)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLPARABEN (UNII: 14255EXE39)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)
- MANGIFERIN (UNII: 1M84LD0UMD)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARETH-100 (UNII: 4OH5W9UM87)
- EDETATE SODIUM (UNII: MP1J8420LU)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".