NDC 20367-111 Rayito De Sol Sunscreen Spf 6
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 20367 - Siscom De Argentina Sa
- 20367-111 - Rayito De Sol Sunscreen Spf 6
Product Packages
NDC Code 20367-111-01
Package Description: 1 TUBE in 1 BOX / 70 g in 1 TUBE
Product Details
What is NDC 20367-111?
What are the uses for Rayito De Sol Sunscreen Spf 6?
Which are Rayito De Sol Sunscreen Spf 6 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Rayito De Sol Sunscreen Spf 6 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CERESIN (UNII: Q1LS2UJO3A)
- PARAFFIN (UNII: I9O0E3H2ZE)
- ZINC STEARATE (UNII: H92E6QA4FV)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- LINALOOL, DL- (UNII: D81QY6I88E)
- COUMARIN (UNII: A4VZ22K1WT)
- .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
- GERANIOL (UNII: L837108USY)
- EUGENOL (UNII: 3T8H1794QW)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- ISOEUGENOL (UNII: 5M0MWY797U)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".