NDC 49825-122 Facescreen Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49825-122?
What are the uses for Facescreen Spf 50?
Which are Facescreen Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Facescreen Spf 50 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:
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CHAMOMILE (UNII: FGL3685T2X)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- RHUS GLABRA BARK (UNII: 7XC0E9WP6U)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
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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".