NDC 42315-672 Moisturising Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42315 - Eshu Pty Ltd
- 42315-672 - Moisturising Sunscreen
Product Packages
NDC Code 42315-672-02
Package Description: 1 BOTTLE in 1 BOX / 100 mL in 1 BOTTLE (42315-672-01)
Product Details
What is NDC 42315-672?
What are the uses for Moisturising Sunscreen Spf 30?
Which are Moisturising Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Moisturising Sunscreen Spf 30 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:
- ALLANTOIN (UNII: 344S277G0Z)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
- LACTIC ACID (UNII: 33X04XA5AT)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- PANTHENOL (UNII: WV9CM0O67Z)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- SERINE (UNII: 452VLY9402)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SORBITOL (UNII: 506T60A25R)
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[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".