NDC 50600-002 Correway Sunscreen (non-waterproof)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50600 - Ningbo Correway Cosmetics Co., Ltd.
- 50600-002 - Correway Sunscreen (non-waterproof)
Product Packages
NDC Code 50600-002-01
Package Description: 42.6 g in 1 TUBE
Product Details
What is NDC 50600-002?
What are the uses for Correway Sunscreen (non-waterproof)?
Which are Correway Sunscreen (non-waterproof) 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)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Correway Sunscreen (non-waterproof) 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CARBOMER 934 (UNII: Z135WT9208)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIAZOLIDINYLUREA (UNII: H5RIZ3MPW4)
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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".