NDC 76144-256 Paulas Choice Lipscreen Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76144-256?
What are the uses for Paulas Choice Lipscreen Spf 50?
Which are Paulas Choice Lipscreen Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Paulas Choice Lipscreen Spf 50 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:
- WATER (UNII: 059QF0KO0R)
- HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)
- HYDROGENATED OLIVE OIL (UNII: 53839415GI)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CERESIN (UNII: Q1LS2UJO3A)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- COCOA BUTTER (UNII: 512OYT1CRR)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SHEANUT OIL (UNII: O88E196QRF)
- TOCOPHEROL (UNII: R0ZB2556P8)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".