NDC 52554-1113 Intensive Cover Blemish Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 52554-1113?
What are the uses for Intensive Cover Blemish Balm?
Which are Intensive Cover Blemish Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Intensive Cover Blemish Balm 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)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- TALC (UNII: 7SEV7J4R1U)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
* 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".