NDC 81129-001 Koru Performance Sunscreen Spf40
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 81129-001?
What are the uses for Koru Performance Sunscreen Spf40?
Which are Koru Performance Sunscreen Spf40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Koru Performance Sunscreen Spf40 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:
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- PROPANEDIOL DICAPRYLATE (UNII: C577OMC6UH)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BATILOL (UNII: 39YR661C4U)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- ETHYL FERULATE (UNII: 5B8915UELW)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- NEOPENTYL GLYCOL DICAPRATE (UNII: 77T908SE82)
- CERESIN (UNII: Q1LS2UJO3A)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PROPANEDIOL (UNII: 5965N8W85T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
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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".