NDC 20367-134 Rayito De Sol Spf 35
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 20367 - Siscom De Argentina S.a.
- 20367-134 - Rayito De Sol
Product Packages
NDC Code 20367-134-01
Package Description: 200 mL in 1 BOTTLE
Product Details
What is NDC 20367-134?
What are the uses for Rayito De Sol Spf 35?
Which are Rayito De Sol Spf 35 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Rayito De Sol Spf 35 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:
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ALLANTOIN (UNII: 344S277G0Z)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- COUMARIN (UNII: A4VZ22K1WT)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EUGENOL (UNII: 3T8H1794QW)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- GERANIOL (UNII: L837108USY)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HEXADECYL POVIDONE (4 HEXADECYL BRANCHES/REPEAT) (UNII: AG75W62QYU)
- IMIDUREA (UNII: M629807ATL)
- ISOCETYL STEAROYL STEARATE (UNII: IJV4LS383R)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- MINERAL OIL (UNII: T5L8T28FGP)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V)
- WATER (UNII: 059QF0KO0R)
- BUTYL ACRYLATE (UNII: 705NM8U35V)
- N-VINYLPYRROLIDINONE (UNII: 76H9G81541)
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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".