NDC 82723-001 Face Spf 47 Setting
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82723 - Aopline Health Industry Technology (guangzhou) Co., Ltd.
- 82723-001 - Face Spf 47 Setting
Product Packages
NDC Code 82723-001-01
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 82723-001?
What are the uses for Face Spf 47 Setting?
Which are Face Spf 47 Setting UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Face Spf 47 Setting 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:
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALCOHOL (UNII: 3K9958V90M)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- HYALURONIC ACID (UNII: S270N0TRQY)
- PEPPERMINT (UNII: V95R5KMY2B)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- NIACINAMIDE (UNII: 25X51I8RD4)
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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".