NDC 13537-270 Lbel Maximum Comfort And Long-lasting Foundation Spf 10 (medium 5) - Brown
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-270 - Lbel Maximum Comfort And Long-lasting Foundation Spf 10
Product Packages
NDC Code 13537-270-18
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 30 mL in 1 BOTTLE, PLASTIC (13537-270-17)
NDC Code 13537-270-20
Package Description: 1 TUBE in 1 BOX / 3 mL in 1 TUBE (13537-270-19)
Product Details
What is NDC 13537-270?
What are the uses for Lbel Maximum Comfort And Long-lasting Foundation Spf 10 (medium 5) - Brown?
Which are Lbel Maximum Comfort And Long-lasting Foundation Spf 10 (medium 5) - Brown 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 Lbel Maximum Comfort And Long-lasting Foundation Spf 10 (medium 5) - Brown 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 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BIS-PEG-18 METHYL ETHER DIMETHYL SILANE (UNII: OEB4R3WW9C)
- PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
- GLYCERIN (UNII: PDC6A3C0OX)
- OLETH-5 (UNII: 1GH33785AY)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MICA (UNII: V8A1AW0880)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- 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".