Label: DR. DREAM COLD PLAZMA WHITENING SERUM- witch hazel liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53077-7001-1 - Packager: Dr. Dream Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated September 25, 2012
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- ACTIVE INGREDIENT
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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
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. DREAM COLD PLAZMA WHITENING SERUM
witch hazel liquidProduct 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)