NDC 13537-152 Esika Natural Care
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 13537-152?
What are the uses for Esika Natural Care?
Which are Esika Natural Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Esika Natural Care 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PAPAIN (UNII: A236A06Y32)
- TROLAMINE (UNII: 9O3K93S3TK)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ROSA MOSCHATA SEED OIL (UNII: T031ZE559T)
- UREA (UNII: 8W8T17847W)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POTASSIUM LACTATE (UNII: 87V1KMK4QV)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ALANINE (UNII: OF5P57N2ZX)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- PROLINE (UNII: 9DLQ4CIU6V)
- SERINE (UNII: 452VLY9402)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
* 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".