Label: DR. DREAM URBAN PROTECTIVE ADVANCED BB- witch hazel cream
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Contains inactivated NDC Code(s)
NDC Code(s): 53077-8001-1 - 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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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
water, butylene glycol, glycerin, cetyl ethylhexanoate, titanium dioxide, hexyl laurate, cetyl peg/ppg-10/1 dimethicone, caprylic/capric triglyceride, isostearyl isostearate, silica, dimethicone/'vinyl dimethicone crosspolymer, dimethicone, caprylyl methicone, magnesium sulfate, sorbitan sesquioleate, zinc stearate, ozokerite, iron oxides, cyclopentasiloxane, disteardimonium hectorite, polyglyceryl-4 isostearate, microcrystalline, wax, silica dimethyl silylate, panthenol, quaternium-18 bentinite, cyclohexasiloxane, CI 77491, talc, caprylyl glycol, triethoxycaprylylsilane, ci 77499, allantoin, licorice root extract, phellinus linteus extract, portulaca oleracea extract, tocopheryl acetate, ci 77003, hydroxyethylcellulose, caprylhydroxamic acid, mica
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. DREAM URBAN PROTECTIVE ADVANCED BB
witch hazel creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53077-8001 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 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:53077-8001-1 30 mL in 1 TUBE 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(53077-8001)
