NDC 59779-968 Daily Facial Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59779-968?
What are the uses for Daily Facial Moisturizer?
Which are Daily Facial Moisturizer 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)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Daily Facial Moisturizer 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)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- UNDECYLCRYLENE DIMETHICONE (10000 MW) (UNII: HA26P2LA4P)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PEG-100 STEARATE (UNII: YD01N1999R)
- METHYL METHACRYLATE (UNII: 196OC77688)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TRIETHANOLAMINE LACTATE (UNII: 064C51N81O)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".