THE BARAFU INTENSIVE SERUM- panthenol, allantoin, adenosine liquid 
Bioresource Co., Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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The Barafu Intensive Serum

Active Ingredients

Panthenol (0.5%)
Allantoin (0.2%)
Adenosine (0.04%)

Purpose

skin protectant

Keep out of reach of children

 Do not swallow. In case of accidental ingestion, seek professional assistance.

Warnings

For external use only
Do not use when Your skin is red, inflamed, irritated or painful
When using this product
 Do not apply on other parts of the body
 Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
 Do not apply directly to wound or open cut.
Stop use and ask doctor if rash or irritation on skin develops and lasts.

Store at room temperature

Uses

Moisturizes and helps to reduce and soften wrinkles. Keep skin look visibly bright, radiant, and smooth.

Directions

Apply the adequate amount on face and neck in the morning and evening twice a day. Use as a night serum as usual moisturizer.

Inactive Ingredients

Water, Mesembryanthemum Crystallimum Extract, Hydroxyethyl Urea, Glycerin, Arbutin, Cyclopentasiloxane, Betaine, Butylene Glycol, Caprylic/Capric Triglyceride, Cyclohexasiloxane, Tuber Melanosporum Extract, Hydrogenated Coconut oil, Benzyl Glycol, Sodium Polyacrylate, Propanediol, PEG-40 Hydrogenated Castor Oil, PPG-26-Buteth-26, Hydrogenated Polydecene, Xanthan Gum, Mica, Dimethicone, Tocopheryl Acetate, Trideceth-6, Titanium Dioxide, Butoxydiglycol, Hydrolyzed Glycosaminoglycans, Fragrance, Raspberry Ketone, Disodium EDTA, Melia Azadirachta Flower Extract, Melia Azadirachta Leaf Extract, Sodium Hyaluronate, Phenoxyethanol, Sodium Oleate, Glycine Soja (Soybean) Oil, Hydrogenated Lecithin, Acetyl Hexapeptide-8

The Barafu Intensive Serum

barafu intensive serum

THE BARAFU INTENSIVE SERUM 
panthenol, allantoin, adenosine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71099-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Panthenol (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) Panthenol0.15 g  in 30 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.06 g  in 30 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.012 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71099-100-021 in 1 PACKAGE12/05/2016
1NDC:71099-100-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/05/2016
Labeler - Bioresource Co., Ltd (689854958)
Registrant - Bioresource Co., Ltd (689854958)
Establishment
NameAddressID/FEIBusiness Operations
Bioresource Co., Ltd689854958manufacture(71099-100)

Revised: 12/2016
Document Id: 6b9065a5-6139-415d-962e-2a26d1b1582a
Set id: 9e4e5bc1-1cf6-4bff-ab10-790ef326889a
Version: 1
Effective Time: 20161205
 
Bioresource Co., Ltd