NDC 51389-210 Laura Geller Spackle Broad Spectrum Spf 30 Protective Under Make-up Primer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51389 - Laura Geller Beauty, Llc
- 51389-210 - Laura Geller Spackle Broad Spectrum Spf 30 Protective Under Make-up Primer
Product Packages
NDC Code 51389-210-00
Package Description: 1 TUBE in 1 PACKAGE / 59 mL in 1 TUBE
Product Details
What is NDC 51389-210?
What are the uses for Laura Geller Spackle Broad Spectrum Spf 30 Protective Under Make-up Primer?
Which are Laura Geller Spackle Broad Spectrum Spf 30 Protective Under Make-up Primer UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Laura Geller Spackle Broad Spectrum Spf 30 Protective Under Make-up Primer 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- MICA (UNII: V8A1AW0880)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GINKGO (UNII: 19FUJ2C58T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- LENTIL (UNII: 6O38V6B52O)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DECYLENE GLYCOL (UNII: S57M60MI88)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".