NDC 63730-171 The Cure Sheer Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63730-171?
What are the uses for The Cure Sheer Cream?
Which are The Cure Sheer Cream 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)
Which are The Cure Sheer Cream 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)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CAPRYLIC/CAPRIC MONO/DIGLYCERIDES (UNII: U72Q2I8C85)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- GLYCERIN (UNII: PDC6A3C0OX)
- WAX, YELLOW (UNII: 2ZA36H0S2V)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- UREA (UNII: 8W8T17847W)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SERINE (UNII: 452VLY9402)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SORBITOL (UNII: 506T60A25R)
- ALLANTOIN (UNII: 344S277G0Z)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PALMITIC ACID (UNII: 2V16EO95H1)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER 934 (UNII: Z135WT9208)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TROLAMINE (UNII: 9O3K93S3TK)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
* 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".