NDC 10096-0241 Anew Solar Advance Eye And Lip Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10096 - Avon Products, Inc.
- 10096-0241 - Anew Solar Advance
Product Packages
NDC Code 10096-0241-3
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 5 g in 1 TUBE, WITH APPLICATOR (10096-0241-1)
NDC Code 10096-0241-3
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 5 g in 1 TUBE, WITH APPLICATOR (10096-0241-2)
Product Details
What is NDC 10096-0241?
What are the uses for Anew Solar Advance Eye And Lip Sunscreen?
Which are Anew Solar Advance Eye And Lip Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Anew Solar Advance Eye And Lip 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:
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
- MICA (UNII: V8A1AW0880)
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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".