NDC 76077-200 Novana Moisturizing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76077 - Novana Medical Llc
- 76077-200 - Novana Moisturizing
Product Packages
NDC Code 76077-200-04
Package Description: 120 mL in 1 TUBE
NDC Code 76077-200-07
Package Description: 210 mL in 1 TUBE
NDC Code 76077-200-09
Package Description: 270 mL in 1 TUBE
Product Details
What is NDC 76077-200?
What are the uses for Novana Moisturizing?
Which are Novana Moisturizing UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Novana Moisturizing 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)
- LANOLIN (UNII: 7EV65EAW6H)
- COD LIVER OIL (UNII: BBL281NWFG)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* 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".