NDC 72805-071 Mychelle Dermaceuticals Sun Shield Spf 50 Medium/dark Protect
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72805 - French Transit, Ltd.
- 72805-071 - Mychelle Dermaceuticals Sun Shield Spf 50 Medium/dark
Product Packages
NDC Code 72805-071-31
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 72805-071?
What are the uses for Mychelle Dermaceuticals Sun Shield Spf 50 Medium/dark Protect?
Which are Mychelle Dermaceuticals Sun Shield Spf 50 Medium/dark 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 Medium/dark 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)
- 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- 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)
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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".