NDC 69096-8001 Linea Jose Ignacio For Face Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 69096-8001?
Which are Linea Jose Ignacio For Face Sunscreen Broad Spectrum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Linea Jose Ignacio For Face Sunscreen Broad Spectrum 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:
- CARBOMER 940 (UNII: 4Q93RCW27E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
- LEMON PEEL (UNII: 72O054U628)
- LYCIUM BARBARUM ROOT BARK (UNII: 766SVR5GCU)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PANTHENOL (UNII: WV9CM0O67Z)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ALLANTOIN (UNII: 344S277G0Z)
- ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)
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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".