Label: DIPHENHYDRAMINE HCL AND IBUPROFEN capsule, liquid filled

  • NDC Code(s): 58602-814-10, 58602-814-12, 58602-814-18, 58602-814-23, view more
    58602-814-30, 58602-814-73
  • Packager: Aurohealth LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated February 21, 2022

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

  • Drug Facts

    Active ingredients
    (in each capsule)

    Diphenhydramine hydrochloride USP 25 mg
    Solubilized ibuprofen equal to 200 mg ibuprofen USP (NSAID)*
    (present as the free acid and potassium salt)
    *nonsteroidal anti-inflammatory drug

  • Purposes

    Nighttime sleep-aid
    Pain reliever

  • Uses

    • for relief of occasional sleeplessness when associated with minor aches and pains
    • helps you fall asleep and stay asleep
  • Warnings

    Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:


    • hives
    • facial swelling
    • asthma (wheezing)
    • shock
    • skin reddening
    • rash
    • blisters

    If an allergic reaction occurs, stop use and seek medical help right away.


    Stomach bleeding warning:
    This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you

    • are age 60 or older
    • have had stomach ulcers or bleeding problems
    • take a blood thinning (anticoagulant) or steroid drug
    • take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
    • have 3 or more alcoholic drinks every day while using this product
    • take more or for a longer time than directed.

    Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

  • Do not use


    • if you have ever had an allergic reaction to any other pain reliever/fever reducer
    • unless you have time for a full night's sleep
    • in children under 12 years of age
    • right before or after heart surgery
    • with any other product containing diphenhydramine, even one used on skin
    • if you have sleeplessness without pain
  • Ask a doctor before use if


    • stomach bleeding warning applies to you
    • you have problems or serious side effects from taking pain relievers or fever reducers
    • you have a history of stomach problems, such as heartburn
    • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke
    • you are taking a diuretic
    • you have a breathing problem such as emphysema or chronic bronchitis
    • you have glaucoma
    • you have trouble urinating due to an enlarged prostate gland
  • Ask a doctor or pharmacist before use if you are


    • taking sedatives or tranquilizers, or any other sleep-aid
    • under a doctor's care for any continuing medical illness
    • taking any other antihistamines
    • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
    • taking any other drug
  • When using this product


    • drowsiness will occur
    • avoid alcoholic drinks
    • do not drive a motor vehicle or operate machinery
    • take with food or milk if stomach upset occurs
  • Stop use and ask a doctor if


    • you experience any of the following signs of stomach bleeding:
      • feel faint
      • vomit blood
      • have bloody or black stools
      • have stomach pain that does not get better
    • you have symptoms of heart problems or stroke:
      • chest pain
      • trouble breathing
      • weakness in one part or side of body
      • slurred speech
      • leg swelling
    • pain gets worse or lasts more than 10 days
    • sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of a serious underlying medical illness.
    • redness or swelling is present in the painful area
    • any new symptoms appear
  • If pregnant or breast-feeding,

    ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

  • 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]

  • Directions


    • do not take more than directed
    • adults and children 12 years and over: take 2 capsules at bedtime
    • do not take more than 2 capsules in 24 hours

    Other information

    • each capsule contains: potassium 20 mg
    • read all warnings and directions before use. Keep carton.
    • store at 20° to 25°C (68° to 77°F)
    • avoid excessive heat above 40°C (104°F)
    • protect from light
    • Organic Impurities Test is Pending
    • Meets USP dissolution test 2

  • Inactive ingredients

    D&C Red No.33, gelatin, hypromellose, isopropyl alcohol, Neelicert FD&C Blue No.1, polyethylene glycol, propylene glycol, potassium hydroxide, povidone, purified water, sorbitol sorbitan solution, titanium dioxide.

    Questions or comments?

    Call 1-855-274-4122 (Monday – Friday 8:30 AM to 5:00 PM EST)

    Distributed by:
    AUROHEALTH LLC
    279 Princeton-Hightstown Road
    East Windsor, NJ 08520

    Made in India

    Code No.: TS/DRUGS/22/2009

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Label

    NDC 58602-814-73
    Diphenhydramine
    HCl and Ibuprofen
    Capsules USP
    25 mg/200 mg
    Nighttime Sleep-Aid/
    Pain Reliever (NSAID)
    20 Liquid Filled Capsules
    READ AND KEEP CARTON FOR COMPLETE
    WARNINGS AND INFORMATION
    AUROHEALTH

    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Label



  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Carton Label

    NDC 58602-814-73
    Diphenhydramine HCl
    and Ibuprofen Capsules USP
    25 mg/200 mg
    Nighttime Sleep-Aid/Pain Reliever (NSAID)
    AUROHEALTH                     20 Liquid Filled Capsules

    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Carton Label

  • INGREDIENTS AND APPEARANCE
    DIPHENHYDRAMINE HCL AND IBUPROFEN 
    diphenhydramine hcl and ibuprofen capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58602-814
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    1,4-SORBITAN (UNII: AV0YTZ4E6J)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    GELATIN TYPE B BOVINE (160 BLOOM) (UNII: 1T8387508X)  
    HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MANNITOL (UNII: 3OWL53L36A)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    POVIDONE K30 (UNII: U725QWY32X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorBLUEScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code DHI25
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58602-814-731 in 1 CARTON02/14/2019
    120 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:58602-814-101 in 1 CARTON02/14/2019
    232 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:58602-814-121 in 1 CARTON02/14/2019
    340 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:58602-814-181 in 1 CARTON02/14/2019
    480 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:58602-814-23120 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2019
    6NDC:58602-814-30160 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21067602/14/2019
    Labeler - Aurohealth LLC (078728447)
    Establishment
    NameAddressID/FEIBusiness Operations
    APL HEALTHCARE LIMITED650844777ANALYSIS(58602-814) , MANUFACTURE(58602-814)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurobindo Pharma Limited650381903ANALYSIS(58602-814) , MANUFACTURE(58602-814)