NDC | 59915-3001-1 |
Set ID | 54927f93-b22a-4cea-bfa3-c13b5361a2ae |
Category | HUMAN OTC DRUG LABEL |
Packager | Conju Inc |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredient: water, titanium dioxide,cyclopentasiloxzne, ethylhexyl methoxycinnamate,propylene glycol, cyclohexasiloxane, butylene glycol dicaprylate/dicaprate, cetyl/peg/ppe-10/1 dimethicone, dimethicone,hexyl laurate, arbutin, tale, PEG-10 dimethicone, panax ginseng root extract, sorbitan, olivate, magnesium sulfate, sorbitan sesquioleate, disteardimonium hectorite,quaternium-19bentonite, chamomilla recutita (matricaria) flower extract, silica, triethyl citrate, allantoin, tocopheryl acetate, dipotassium clycyrrhizate, iron oxide (CI 77492), iron oxide (CI 77491), iron oxide (CI 77499), ultramarines (CI 77007), triethoxycaprylylsilane, propylparaben, methylparaben, phenoxyethanol, adenosine, mica, sodim hyaluronate
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CONJU PRINCESS BB
arbutin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59915-3001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 10.15 mL in 100 mL ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN 2 mL in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) OCTINOXATE (UNII: 4Y5P7MUD51) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CYCLOMETHICONE 6 (UNII: XHK3U310BA) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) HEXYL LAURATE (UNII: 4CG9F9W01Q) TALC (UNII: 7SEV7J4R1U) ASIAN GINSENG (UNII: CUQ3A77YXI) SORBITAN OLIVATE (UNII: MDL271E3GR) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) HECTORITE (UNII: 08X4KI73EZ) BENTONITE (UNII: A3N5ZCN45C) CHAMOMILE (UNII: FGL3685T2X) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) ALLANTOIN (UNII: 344S277G0Z) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) LICORICE (UNII: 61ZBX54883) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) OCTYLTRIETHOXYSILANE (UNII: LDC331P08E) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYLPARABEN (UNII: A2I8C7HI9T) PHENOXYETHANOL (UNII: HIE492ZZ3T) MICA (UNII: V8A1AW0880) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59915-3001-1 1 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/30/2010 Labeler - Conju Inc (012345486)