NDC 76214-004 Agave Cactus Light
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 76214-004?
What are the uses for Agave Cactus Light?
Which are Agave Cactus Light UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Agave Cactus Light 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)
- AGAVE TEQUILANA LEAF (UNII: 05545M0E3M)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ARBUTIN (UNII: C5INA23HXF)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- BETAINE (UNII: 3SCV180C9W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MAACKIA FLORIBUNDA STEM (UNII: 84UXW52K8Y)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- ADENOSINE (UNII: K72T3FS567)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Agave Cactus Light?
- RxCUI: 200010 - dimethicone 1 % Topical Cream
- RxCUI: 200010 - dimethicone 10 MG/ML Topical Cream
* 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".