DR. DREAM COLD PLAZMA WHITENING SERUM- witch hazel liquid

Dr. Dream Cold Plazma Whitening Serum by

Drug Labeling and Warnings

Dr. Dream Cold Plazma Whitening Serum by is a Otc medication manufactured, distributed, or labeled by Dr. Dream Inc, New & New Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

witch hazel

INACTIVE INGREDIENT

Galactomyces Ferment Filtrate, water, butylene glycol, glycerin, niacinamide, squalane, methyl glucose sesquistearate, olive fruit oil, caprylic/capric triglyceride, tocopheryl acetate, panthenol, polysorbate 80, sodium polyacrylate, caprylyl glycol, dimethicone, pentylene glycol, sorbitan sesquioleate, cyclopentasiloxane, torreya nucifera extract, cornus kousa extract, rosa mutiflora fruit extract, chloranthus glaber extract, musa basjoo extract, trideceth-6, rh-oligopeptide-1, dipotassium glycyrrhizate, acetyl hexapeptide-8, arginine, palmitoyl oligopeptide, palmitoyl tetrapeptide-7, caprylhydroxamic acid, disodium edta, lecithin, sodium phosphate, peg/ppg-18/19\8 dimethicone, rh-oligopeptide-2, rh-polypeptide-1, rh-polypeptide-11, lavender oil, cymbopogon schoenarthus oil, abies sibirica oil, orange peel oil, allantoin, amyris balsamifera bark oil, clary oil, rh-polypeptide-60, rh-polypeptide-10, rh-polypeptide-9

PURPOSE

whitening care

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

After applying dr. dream Advance Facial Treatment Toner, take out the proper amount and apply it to your face as massaging to be well absorbed. There would be better effect if you apply it twice a day in the morning and evening.

WARNINGS

When using this product
- keep out of eyes, ears, and mouth.  If contact occurs, rinse with plenty of cold water right away and contact a physician.  If swallowing, drink plenty of water and contact a physician

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. DREAM COLD PLAZMA WHITENING SERUM 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53077-7001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	0.1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
POLYSORBATE 60 (UNII: CAL22UVI4M)
GLYCERIN (UNII: PDC6A3C0OX)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
ADENOSINE (UNII: K72T3FS567)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
NEOPENTYL GLYCOL (UNII: QI80HXD6S5)
BLACK OLIVE (UNII: 2M6QWV94OC)
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)
ABIES SIBIRICA LEAF OIL (UNII: XRY0V4VZKZ)
ORANGE (UNII: 5EVU04N5QU)
AMYRIS BALSAMIFERA OIL (UNII: I1BJ961J2E)
CLARY SAGE OIL (UNII: 87L0D4U3M0)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
SODIUM PHOSPHATE (UNII: SE337SVY37)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
THIOREDOXIN (UNII: XJZ418133Z)
PREZATIDE COPPER (UNII: 6BJQ43T1I9)
PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
GLYCINE (UNII: TE7660XO1C)
GLUTAMINE (UNII: 0RH81L854J)
LYSINE (UNII: K3Z4F929H6)
LEUCINE (UNII: GMW67QNF9C)
METHIONINE (UNII: AE28F7PNPL)
VALINE (UNII: HG18B9YRS7)
SERINE (UNII: 452VLY9402)
CYSTEINE (UNII: K848JZ4886)
CYSTINE (UNII: 48TCX9A1VT)
ASPARAGINE (UNII: 5Z33R5TKO7)
ALANINE (UNII: OF5P57N2ZX)
ARGININE (UNII: 94ZLA3W45F)
ORNITHINE (UNII: E524N2IXA3)
ISOLEUCINE (UNII: 04Y7590D77)
TYROSINE (UNII: 42HK56048U)
THREONINE (UNII: 2ZD004190S)
TRYPTOPHAN (UNII: 8DUH1N11BX)
PHENYLALANINE (UNII: 47E5O17Y3R)
PROLINE (UNII: 9DLQ4CIU6V)
HISTIDINE (UNII: 4QD397987E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53077-7001-1	50 mL in 1 BOTTLE, GLASS

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	09/25/2012

Labeler - Dr. Dream Inc (557821161)

Registrant - Dr. Dream Inc (557821161)

Establishment
Name	Address	ID/FEI	Business Operations
New & New Co., Ltd		557821160	manufacture(53077-7001)