NDC 43948-1101 Dr. Young 2p Pearl Brightening Balm Spf35 Pa
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43948 - The Doctors Cosmetics Co., Ltd
- 43948-1101 - Dr. Young 2p Pearl Brightening Balm Spf35 Pa
Product Packages
NDC Code 43948-1101-1
Package Description: 30 mL in 1 TUBE
Product Details
What is NDC 43948-1101?
What are the uses for Dr. Young 2p Pearl Brightening Balm Spf35 Pa?
Which are Dr. Young 2p Pearl Brightening Balm Spf35 Pa UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Dr. Young 2p Pearl Brightening Balm Spf35 Pa 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- BENTONITE (UNII: A3N5ZCN45C)
- CHRYSANTHELLUM INDICUM FLOWER OIL (UNII: HJ299SUZ05)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- MAGNOLIA LILIIFLORA FLOWER (UNII: SVM28292LH)
- CONVALLARIA MAJALIS BULB (UNII: 261W7X975U)
- SHEA BUTTER (UNII: K49155WL9Y)
- MAGNOLIA KOBUS BARK (UNII: 54LVP49595)
- THUJOPSIS DOLABRATA WHOLE (UNII: Q190548W6J)
- BANCHA TEA LEAF/TWIG (UNII: EWI42IEH1C)
- PUMMELO (UNII: ET1TN5W71X)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ALCEA ROSEA FLOWER (UNII: 1250O8MKPZ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- LILIUM CANDIDUM FLOWER (UNII: COV655U2CJ)
- CERAMIDE 3 (UNII: 4370DF050B)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* 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".