NDC 72805-111 Mychelle Dermaceuticals Sun Shield Spf 50 Tinted Protect
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72805 - French Transit, Ltd.
- 72805-111 - Mychelle Dermaceuticals Sun Shield Spf 50 Tinted
Product Packages
NDC Code 72805-111-15
Package Description: 1 CONTAINER in 1 BOX / 15 g in 1 CONTAINER
Product Details
What is NDC 72805-111?
What are the uses for Mychelle Dermaceuticals Sun Shield Spf 50 Tinted Protect?
Which are Mychelle Dermaceuticals Sun Shield Spf 50 Tinted 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 Tinted 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- LEVOMENOL (UNII: 24WE03BX2T)
- SHEA BUTTER (UNII: K49155WL9Y)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- CANDELILLA WAX (UNII: WL0328HX19)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- OCTYLDODECYL OLEATE (UNII: MCA43PK7MH)
- ORYZANOL (UNII: SST9XCL51M)
- RICE BRAN OIL (UNII: LZO6K1506A)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- CHIA SEED OIL (UNII: MC2LH51BO7)
- JOJOBA OIL (UNII: 724GKU717M)
- COCOA BUTTER (UNII: 512OYT1CRR)
- 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".