NDC 49825-121 Ray Defense Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49825-121?
What are the uses for Ray Defense Spf 30 Sunscreen?
Which are Ray Defense Spf 30 Sunscreen 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Ray Defense Spf 30 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHAMOMILE (UNII: FGL3685T2X)
- CITRUS AURANTIUM FLOWER OIL (UNII: D4BGE91OXH)
- CITRUS RETICULATA LEAF OIL (UNII: 1515UE78IH)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- SAGE OIL (UNII: U27K0H1H2O)
- CLARY SAGE OIL (UNII: 87L0D4U3M0)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- EDETATE SODIUM (UNII: MP1J8420LU)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
* 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".