NDC 71099-100 The Barafu Intensive Serum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71099 - Bioresource Co., Ltd
- 71099-100 - The Barafu Intensive Serum
Product Packages
NDC Code 71099-100-02
Package Description: 1 BOTTLE in 1 PACKAGE / 30 mL in 1 BOTTLE (71099-100-01)
Product Details
What is NDC 71099-100?
What are the uses for The Barafu Intensive Serum?
Which are The Barafu Intensive Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are The Barafu Intensive Serum 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)
- MESEMBRYANTHEMUM CRYSTALLINUM WHOLE (UNII: KFD19SXO43)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
- GLYCERIN (UNII: PDC6A3C0OX)
- ARBUTIN (UNII: C5INA23HXF)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BETAINE (UNII: 3SCV180C9W)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- BLACK TRUFFLE (UNII: 6G823JVR48)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- ETHYLENE GLYCOL MONOBENZYL ETHER (UNII: 06S8147L47)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- PROPANEDIOL (UNII: 5965N8W85T)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MICA (UNII: V8A1AW0880)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- DIETHYLENE GLYCOL MONOBUTYL ETHER (UNII: 9TB90IYC0E)
- HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) (UNII: 997385V0VV)
- 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- AZADIRACHTA INDICA FLOWER (UNII: 3TE8A92UPM)
- AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM OLEATE (UNII: 399SL044HN)
- SOYBEAN OIL (UNII: 241ATL177A)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
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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".