Label: NMNQUIL- nighttime sleep aid capsule

  • 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 April 24, 2023

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  • PURPOSE

    for relief of occasional sleeplessness

  • ACTIVE INGREDIENT

    Diphenhydramine HCL 50mg - Nighttime Sleep Aid

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose get medical help or contact a Poison Control Center right away.

  • INDICATIONS & USAGE

    adults and children 12 years of age and over: take 2 capsules (50 mg) at bedtime if needed, or as directed by a doctor

  • INACTIVE INGREDIENT

    Hypromellose (capsule)

    NMN (nicotinamide mononucleotide)

    Rice Flour

  • DOSAGE & ADMINISTRATION

    take 2 capsules (50 mg) at bedtime if needed

  • WARNINGS

    Do not use with any other product containing diphenhydramine, even one used on skin in children under 12 years of age ■ Ask a doctor before use if you have and/or use glaucoma or a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland sedatives or tranquilizers (in each capsule) ■ When using this product avoid alcoholic drinks Stop use and ask a doctor if sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness If pregnant or breast-feeding, ask a health professional before use Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)

  • PRINCIPAL DISPLAY PANEL

    NMNQuil Inactive ingredients: Capsule (190mg) NMN (500mg) Rice Flour (100mg) Non-Habit Forming 60 VEGAN CAPSULES NMNIGHTTIME SLEEP-AID Drug Facts Active ingredient Purpose Diphenhydramine HCL 25mg. Nighttime sleep-aid Use for relief of occasional sleeplessness Warnings with any other product containing diphenhydramine, even one used on skin in children under 12 years of age Do not use: ■ ■ Ask a doctor before use if you have and/or use glaucoma or a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland sedatives or tranquilizers (in each capsule) ■ When using this product avoid alcoholic drinks Stop use and ask a doctor if sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness If pregnant or breast-feeding, ask a health professional before use Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222) adults and children 12 years of age and over: take 2 capsules (50 mg) at bedtime if needed, or as directed by a doctor Directions Drug Facts (continued) Inactive ingredients (in each capsule) NMN (Nicotinamide mononucleotide) 250mg Rice Flour 50mg Questions or comments? 1-800-872-9500 TAMPER EVIDENT: DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING Hypromellose (Capsule) 95mg NDC 73769-200-60 ■■ Manufactured by Nature’s Fusions Orem, Utah 84057 www.naturesfusions.com

    NMNQuil

  • INGREDIENTS AND APPEARANCE
    NMNQUIL 
    nighttime sleep aid capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73769-200
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    NICOTINAMIDE MONONUCLEOTIDE (UNII: 2KG6QX4W0V)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    STARCH, RICE (UNII: 4DGK8B7I3S)  
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeCAPSULE (Size 0) Size22mm
    FlavorVANILLA (No flavor) Imprint Code None
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73769-200-6060 in 1 BOTTLE; Type 0: Not a Combination Product04/26/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM01004/26/2023
    Labeler - NATURE'S FUSIONS, LLC (051472644)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURE'S FUSIONS, LLC051472644manufacture(73769-200)