Label: REUS NR capsule

  • NDC Code(s): 83663-003-01, 83663-003-02
  • Packager: REUS POLSKA SP Z O O
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated September 15, 2023

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    NMN (B-Nicotinamide Mononucleotide) 600mg

  • DO NOT USE

    1. as aubstitute for sleep. This product is intended for occastional use only.

    2. In children under 12 years of age

  • INACTIVE INGREDIENT

    Rice flour, microcrystalline cellulose, silicon dioxide, magnesium stearate

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of Children.

  • PREGNANCY OR BREAST FEEDING

    If pregrant or breast feeding, ask a health professional before use.

  • WARNINGS

    Do Not Use

    as substitute for sleep. This product is intended for occasional use only.

  • QUESTIONS

    Call toll-free 1-855-874-0970 weekdays

  • STORAGE AND HANDLING

    Store id a dry place at 15 - 30C (59 - 86F)

    Avoid excessive heat (greater than 100F) or humidity

  • WARNINGS AND PRECAUTIONS

    Adults and children 12 years of age and over: take 2 capsules not more often than every 3 to 4 hours

  • DOSAGE & ADMINISTRATION

    Each capsule contains Quercetin Phytosome 250mb, Trans-Resveratrol 150 mg

  • INDICATIONS & USAGE

    Adults and children 12 years of age and over: take 2 capsules not more often than every 3 to 4 hours

  • PURPOSE

    Helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness.

  • PRINCIPAL DISPLAY PANEL

    NaMN

  • INGREDIENTS AND APPEARANCE
    REUS NR 
    reus nr capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83663-003
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NICOTINAMIDE MONONUCLEOTIDE (UNII: 2KG6QX4W0V) (NICOTINAMIDE MONONUCLEOTIDE - UNII:2KG6QX4W0V) NICOTINAMIDE MONONUCLEOTIDE600 mg
    Inactive Ingredients
    Ingredient NameStrength
    RESVERATROL (UNII: Q369O8926L) 150 mg
    Product Characteristics
    Colorwhite (WHITE (C48325)) Scoreno score
    ShapeCAPSULE (CAPSULE (C48336)) Size23mm
    FlavorImprint Code 732
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83663-003-0280 in 1 BOTTLE07/20/2023
    180 in 1 BOTTLE
    1NDC:83663-003-0180 in 1 BOTTLE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/20/2023
    Labeler - REUS POLSKA SP Z O O (522592245)