Label: BUENO HYDRO VOLUME LIFT SERUM- dimethicone liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73261-0003-1 - Packager: Bueno MEDITECH
- 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 3, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Aureobasidium Pullulans Ferment Extract,Tuber Melanosporum Extract,Butylene Glycol,Hydrogenated polyisobutene,
1,2-Hexanediol,Panthenol,Dimethicone,Cetearyl Olivate,Sorbitan Olivate,Water,Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer,Arginine,Glutathione,Isohexadecane,Ceteareth-20,Sodium Hyaluronate,Polysorbate 80,Simmondsia Chinensis (Jojoba) Seed Oil,Helianthus Annuus (Sunflower) Seed Oil,Tocopheryl Acetate,Allantoin,Argania Spinosa Kernel Oil,Olea Europaea (Olive) Fruit Oil,Perfume,Adenosine,Ethylhexylglycerin,Disodium EDTA,Olea Europaea (Olive) Husk Oil,
Tocopherol,Anemarrhena Asphodeloides Root Extract,Caprylyl Glycol,Acetyl Octapeptide-3,Acetyl Hexapeptide-8,Acetyl Hexapeptide-22,Oligopeptide-28,sh-Pentapeptide-19,sh-Octapeptide-4,Caffeoyl Tripeptide-1,sh-Decapeptide-7,Sh-Oligopeptide-1
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BUENO HYDRO VOLUME LIFT SERUM
dimethicone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73261-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 2.5 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73261-0003-1 40 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/02/2019 Labeler - Bueno MEDITECH (695687664) Registrant - Bueno MEDITECH (695687664) Establishment Name Address ID/FEI Business Operations Bueno MEDITECH 695687664 label(73261-0003) , manufacture(73261-0003)
