NDC 31190-210 Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 31190 - Shanghai Kejing Cleaning Products Co., Ltd
- 31190-210 - Sunscreen Spf 30
Product Characteristics
Product Packages
NDC Code 31190-210-20
Package Description: 20 mL in 1 BOTTLE
NDC Code 31190-210-30
Package Description: 30 mL in 1 BOTTLE
Product Details
What is NDC 31190-210?
What are the uses for Sunscreen Spf 30?
Which are Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are 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:
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- MYRISTYL PROPIONATE (UNII: P59053E7NJ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
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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".