Label: DR. DREAM ADVANCED FACIAL TREATMENT SERUM- witch hazel cream
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Contains inactivated NDC Code(s)
NDC Code(s): 53077-3001-1 - 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 August 24, 2012
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
bis-PEG-18 methyl ether dimethyl silane, polyglutamic acid, butylene glycol, panthenol, sodium PCA, caprylyl glycol, torreya nucifera extract, cornus kousa extract, rosa multiflora fruit extract, chloranthus glaber extract, musa basjoo extract, musa basjoo extract, rh-oligopeptide-1, acetyl hexapeptide=8, palmitoyl oligopeptice, palmitoyl tetrapeptide-7, polysorbate 80, glycerin, caprylhydroxamic acid, adenosine, ammonium acryloyldimethyltaurate, hydroxyethylcellulose, pentylene glycol, cellulose gum, sodium chondroitin sulfate, lavandula angustifolia oil, cymbopogon schoenanthus oil, abies sibirica oil, citrus auratium dulcis peel oil, amyris balsamifera bark oil, salvia sclarea oil, lecithin, sodium phosphate, sodium hyaluronate, rh-polypeptide-60, rh-polypeptide-9, rh-polypeptide-11, rh-polypeptide-2, rh-polypeptide-1, rh-polypeptide-10, copper tripeptide-1, palmitoyl pentapeptide-4, glycine, glutamine, lysine, leucine, methionine, valine, serine, cysteine, cystine, asparagine, alanine, arginine, ornithine, isoleucine,tyrosine, threonine, tryptophan, phenylalanine, proline, histidine, olea europaea fruit oil, safflower seed oil, glyceryl stearate, beeswax, stearic acid polysorbate 60, cyclopentasiloxane, dimethicone, sorbitan, stearate, peg-100 stearate,
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. DREAM ADVANCED FACIAL TREATMENT SERUM
witch hazel creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53077-3001 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 NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PANTHENOL (UNII: WV9CM0O67Z) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TORREYA NUCIFERA WHOLE (UNII: 91Z68135ZV) ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13) MUSA BASJOO WHOLE (UNII: V3AYC3JL9Y) ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL) 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:53077-3001-1 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 08/24/2012 Labeler - Dr. Dream Inc (557821161) Registrant - Dr. Dream Inc (557821161) Establishment Name Address ID/FEI Business Operations New & New Co., Ltd 557821160 manufacture(53077-3001)