NDC 72805-180 Mychelle Dermaceuticals Sun Shield Spf 50 Light Protect
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72805 - French Transit, Ltd.
- 72805-180 - Mychelle Dermaceuticals Sun Shield Spf 50 Light
Product Packages
NDC Code 72805-180-30
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 72805-180?
What are the uses for Mychelle Dermaceuticals Sun Shield Spf 50 Light Protect?
Which are Mychelle Dermaceuticals Sun Shield Spf 50 Light Protect UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Mychelle Dermaceuticals Sun Shield Spf 50 Light Protect 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)
- BENTONITE (UNII: A3N5ZCN45C)
- LEVOMENOL (UNII: 24WE03BX2T)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- COCO GLUCOSIDE (UNII: ICS790225B)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- ETHYL FERULATE (UNII: 5B8915UELW)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW) (UNII: J2S07SB0YL)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- MALTOSE, UNSPECIFIED FORM (UNII: XJ6S9RV06F)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
* 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".