Label: BIELLEE POLLEN WHITENING WRINKLE TIME REPAIR CREAM- dimethicone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70784-002-01, 70784-002-02 - Packager: NSB CO., LTD.
- 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 June 21, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
WATER
GLYCERIN
DIPROPYLENE GLYCOL
POLLEN EXTRACT
PENTAERYTHRITYL TETRAISOSTEARATE
HYDROGENATED POLYDECENE
MORINDA CITRIFOLIA FRUIT EXTRACT
BUTYLENE GLYCOL
CAPRYLIC/CAPRIC TRIGLYCERIDE
TRIETHYLHEXANOIN
GLYCERYL STEARATE CITRATE
NIACINAMIDE
CETEARYL ALCOHOL
GLYCERYL STEARATE
BEHENYL ALCOHOL
FRAGRANCE
PEG-100 STEARATE
PHENOXYETHANOL
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER
ISOHEXADECANE
ALLANTOIN
XANTHAN GUM
ETHYLHEXYLGLYCERIN
POLYSORBATE80
DISODIUM EDTA
SODIUM HYALURONATE - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BIELLEE POLLEN WHITENING WRINKLE TIME REPAIR CREAM
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70784-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 0.5 mg in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIPROPYLENE GLYCOL (UNII: E107L85C40) BEE POLLEN (UNII: 3729L8MA2C) PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F) HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7) NONI FRUIT (UNII: 7829X3G2X5) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) NIACINAMIDE (UNII: 25X51I8RD4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) DOCOSANOL (UNII: 9G1OE216XY) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) ISOHEXADECANE (UNII: 918X1OUF1E) ALLANTOIN (UNII: 344S277G0Z) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYSORBATE 80 (UNII: 6OZP39ZG8H) EDETATE DISODIUM (UNII: 7FLD91C86K) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70784-002-02 1 in 1 CARTON 06/21/2016 1 NDC:70784-002-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 06/21/2016 Labeler - NSB CO., LTD. (689846922) Registrant - NSB CO., LTD. (689846922) Establishment Name Address ID/FEI Business Operations NSB CO., LTD. 689846922 manufacture(70784-002)