NDC 98132-163 Ready Foundation Fair
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 98132 - Bare Escentuals Beauty Inc.
- 98132-163 - Ready Foundation
Product Packages
NDC Code 98132-163-08
Package Description: 14 g in 1 TRAY
Product Details
What is NDC 98132-163?
What are the uses for Ready Foundation Fair?
Which are Ready Foundation Fair 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)
Which are Ready Foundation Fair 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:
- BORON NITRIDE (UNII: 2U4T60A6YD)
- OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- NYLON-12 (UNII: 446U8J075B)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- ALARIA ESCULENTA (UNII: EJ9JK8J58D)
- BETAINE (UNII: 3SCV180C9W)
- MANNITOL (UNII: 3OWL53L36A)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
- ZINC SULFATE (UNII: 89DS0H96TB)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
* 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".