Label: MECLIZINE HCL 25 MG- meclizine hcl tablet

  • NDC Code(s): 71335-1607-0, 71335-1607-1, 71335-1607-2, 71335-1607-3, view more
    71335-1607-4, 71335-1607-5, 71335-1607-6, 71335-1607-7, 71335-1607-8, 71335-1607-9
  • Packager: Bryant Ranch Prepack
  • This is a repackaged label.
  • Source NDC Code(s): 69618-028
  • 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 October 20, 2020

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

  • Drug Facts

  • Active ingredient (in each tablet)

    Meclizine HCL 25 mg

  • Purpose

    Antiemetic

  • Uses

    • prevents and treats nausea, vomiting or dizziness due to motion sickness
    • for others uses, consult your doctor
  • Warnings

    Ask a doctor before use if you have

    • glaucoma
    • a breathing problem such as emphysema or chronic bronchitis
    • trouble urinating due to an enlarged prostate gland

    Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

    When using this prodcut

    • you may get drowsy
    • avoid alcoholic drinks
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery

    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.

  • ASK DOCTOR

    Ask a doctor before use if you have

    • glaucoma
    • a breathing problem such as emphysema or chronic bronchitis
    • trouble urinating due to an enlarged prostate gland
  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

  • WHEN USING

    When using this product

    • you may get drowsy
    • avoid alcoholic drinks
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery
  • PREGNANCY OR BREAST FEEDING

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

  • 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.

  • Directions

    • take dose one hour before travel starts
    • tablets can be chewed or swallowed whole with water

    adults & children 12 years and over: 1-2 tablets once daily

    children unser 12 years: ask a doctor

  • Other information

    • Phenylketonurics: each tablet contrains: phenylalanine 0.28 mg
    • store at room temperature 15°-30°C (59°-86°F)
    • This is a bulf package. Dispense contents with a child-resistant closure in a tight, light-resistant container as defined in the USP.
  • Inactive ingredients

    aspartame, compressible sugar, croscarmellose sodium, dextrose, FD&C red # 40 (Al-lake), magnesium stearate, microcrystalline cellulose, raspberry flavor

  • Questions or comments?

    call 516-341-0666, 8:30 am - 4:30 pm ET, Monday - Friday

  • SPL UNCLASSIFIED SECTION

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

  • SPL UNCLASSIFIED SECTION

    *Reliable 1 Laboratories LLC is not affiliated with the owner of the trademark BONINE®.

    Distributed by: Reliable 1 Laboratories LLC, Valley Stream, NY 11580

    www.reliable1labs.com

  • HOW SUPPLIED

    Product: 71335-1607

    NDC: 71335-1607-0 120 TABLET in a BOTTLE

    NDC: 71335-1607-1 30 TABLET in a BOTTLE

    NDC: 71335-1607-2 20 TABLET in a BOTTLE

    NDC: 71335-1607-3 25 TABLET in a BOTTLE

    NDC: 71335-1607-4 40 TABLET in a BOTTLE

    NDC: 71335-1607-5 60 TABLET in a BOTTLE

    NDC: 71335-1607-6 90 TABLET in a BOTTLE

    NDC: 71335-1607-7 8 TABLET in a BOTTLE

    NDC: 71335-1607-8 14 TABLET in a BOTTLE

    NDC: 71335-1607-9 10 TABLET in a BOTTLE

  • Meclizine 25MG Chewable

    Label Image
  • INGREDIENTS AND APPEARANCE
    MECLIZINE HCL 25 MG 
    meclizine hcl tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-1607(NDC:69618-028)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    RASPBERRY (UNII: 4N14V5R27W)  
    ASPARTAME (UNII: Z0H242BBR1)  
    SUCROSE (UNII: C151H8M554)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    Product Characteristics
    Colorpink (Light Raspberry color) Score2 pieces
    ShapeROUNDSize8mm
    FlavorRASPBERRYImprint Code AP;115
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71335-1607-910 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    2NDC:71335-1607-690 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    3NDC:71335-1607-130 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    4NDC:71335-1607-78 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    5NDC:71335-1607-440 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    6NDC:71335-1607-560 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    7NDC:71335-1607-220 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    8NDC:71335-1607-814 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    9NDC:71335-1607-325 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    10NDC:71335-1607-0120 in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33611/01/2015
    Labeler - Bryant Ranch Prepack (171714327)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bryant Ranch Prepack171714327REPACK(71335-1607) , RELABEL(71335-1607)