NDC 13537-200 Lbel Filling Effect Foundation Spf 10 (claire 1) - Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-200 - Lbel Filling Effect Foundation Spf 10
Product Packages
NDC Code 13537-200-02
Package Description: 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE (13537-200-01)
NDC Code 13537-200-04
Package Description: 1 TUBE in 1 BOX / 3 mL in 1 TUBE (13537-200-03)
Product Details
What is NDC 13537-200?
What are the uses for Lbel Filling Effect Foundation Spf 10 (claire 1) - Beige?
Which are Lbel Filling Effect Foundation Spf 10 (claire 1) - Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Lbel Filling Effect Foundation Spf 10 (claire 1) - Beige 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)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".