NDC 61619-866 Pro-tect Sunscreen For Professionals
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61619 - A-cute Derm, Incorporated
- 61619-866 - Pro-tect Sunscreen For Professionals
Product Packages
NDC Code 61619-866-01
Package Description: 29.6 mL in 1 BOTTLE, PLASTIC
NDC Code 61619-866-02
Package Description: 59.1 mL in 1 BOTTLE, PLASTIC
NDC Code 61619-866-04
Package Description: 118.3 mL in 1 BOTTLE, PLASTIC
NDC Code 61619-866-08
Package Description: 236.6 mL in 1 BOTTLE, PLASTIC
NDC Code 61619-866-32
Package Description: 946.4 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 61619-866?
What are the uses for Pro-tect Sunscreen For Professionals?
Which are Pro-tect Sunscreen For Professionals UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- MERADIMATE (UNII: J9QGD60OUZ)
- MERADIMATE (UNII: J9QGD60OUZ) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Pro-tect Sunscreen For Professionals 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LANOLIN (UNII: 7EV65EAW6H)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MINERAL OIL (UNII: T5L8T28FGP)
- TALC (UNII: 7SEV7J4R1U)
- TROLAMINE (UNII: 9O3K93S3TK)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL DIMETHICONE 45 (UNII: IK315POC44)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
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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".