Label: NIGHTTIME SLEEP AID- acetaminophen, diphenhydramine tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 December 31, 2022

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  • ACTIVE INGREDIENT

    actives

  • ASK DOCTOR

    ask a doc

  • ASK DOCTOR/PHARMACIST

    ask a doc or pharm

  • DO NOT USE

    do not use

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach

  • PREGNANCY OR BREAST FEEDING

    pregnancy

  • PURPOSE

    Purpose

  • QUESTIONS

    Questions

  • STOP USE

    stop use

  • WHEN USING

    when using

  • OVERDOSAGE

    Overdose

  • WARNINGS

    warnings

  • INACTIVE INGREDIENT

    inactives

  • INDICATIONS & USAGE

    uses

  • STORAGE AND HANDLING

    storage

  • DOSAGE & ADMINISTRATION

    directions

  • PRINCIPAL DISPLAY PANEL

    pdp

  • INGREDIENTS AND APPEARANCE
    NIGHTTIME SLEEP AID 
    acetaminophen, diphenhydramine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69732-005
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeCAPSULESize19mm
    FlavorImprint Code HTP525
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69732-005-0130 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34304/30/2020
    Labeler - Hi-Tech Nutraceuticals, LLC (606221443)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hi-Tech Nutraceuticals, LLC080787135pack(69732-005)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hi-Tech Nutraceuticals, LLC606221443manufacture(69732-005)