THE BARAFU INTENSIVE SERUM- panthenol, allantoin, adenosine liquid

The Barafu Intensive Serum by

Drug Labeling and Warnings

The Barafu Intensive Serum by is a Otc medication manufactured, distributed, or labeled by Bioresource Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

THE BARAFU INTENSIVE SERUM 
panthenol, allantoin, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71099-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Panthenol (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	Panthenol	0.15 g  in 30 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.06 g  in 30 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.012 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71099-100-02	1 in 1 PACKAGE	12/05/2016
1	NDC: 71099-100-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/05/2016

Labeler - Bioresource Co., Ltd (689854958)

Registrant - Bioresource Co., Ltd (689854958)

Establishment
Name	Address	ID/FEI	Business Operations
Bioresource Co., Ltd		689854958	manufacture(71099-100)