Ibuprofen and Diphenhydramine Citrate

Dosage form: tablet
Ingredients: ibuprofen 200mg, diphenhydramine citrate 38mg
Labeler: Dr. Reddy's Laboratories Limited
NDC Code: 55111-565

Ibuprofen and Diphenhydramine Citrate Tablets

DRUG FACTS

ACTIVE INGREDIENTS (IN EACH CAPLET*)

Diphenhydramine citrate USP, 38 mg

Ibuprofen USP, 200 mg (NSAID)**

* capsule-shaped tablets

**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 a nonsteroidal anti-inflammatory drug (NSAID), which may cause 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 an NSAID [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

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 you have
  • a breathing problem such as emphysema or chronic bronchitis
  • problems or serious side effects from taking pain relievers or fever reducers
  • stomach problems that last or come back, such as heartburn, upset stomach, or stomach pain
  • ulcers
  • bleeding problems
  • high blood pressure
  • heart or kidney disease
  • asthma
  • taken a diuretic
  • reached age 60 or older
  • glaucoma
  • 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
  • taking any other drug containing an NSAID (prescription or nonprescription)
  • under a doctor’s care for any continuing medical illness
  • taking any other antihistamines
  • taking a blood thinning (anticoagulant) or steroid drug
  • 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
  • the risk of heart attack or stroke may increase if you use more than directed or for longer than directed

Stop use and ask a doctor if
  • you feel faint, vomit blood, or have bloody or black stools. These are signs of stomach bleeding
  • 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.
  • stomach pain or upset gets worse or lasts
  • 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 during the last 3 months of 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 the reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS
  • do not take more than directed
  • do not take longer than 10 days, unless directed by a doctor (see WARNINGS)
  • adults and children 12 years and over: take 2 caplets at bedtime.
  • do not take more than 2 caplets in 24 hours

OTHER INFORMATION
  • read all warnings and directions before use. Keep carton.
  • store at 20-25°C (68-77°F)
  • avoid excessive heat above 40°C (104°F)

INACTIVE INGREDIENTS

carnauba wax, corn starch, colloidal silicon dioxide, croscarmellose sodium, FD&C blue no. 2, hypromelllose, microcrystalline cellulose, polydextrose, polyethylene glycol 400, pregelatinized starch, sodium lauryl sulfate, stearic acid, titanium dioxide

QUESTIONS OR COMMENTS?

Call 1-888-375-3784

Do Not Use if foil seal under bottle cap imprinted with“SEALED for YOUR PROTECTION”  is broken or missing.

Manufactured for:Dr. Reddy’s Laboratories Limited Bachepalli – 502 325 INDIA.

PRINCIPAL DISPLAY PANEL

Pouch label:

DR. REDDY'S

NDC 55111-565-92

Count :2,500 Tablets

Ibuprofen Diphenhydramine Citrate Tablets 200 mg/38 mg

Batch No. :

Mfg. Date :

Repack Before :

Expiration Date :

Store at 20°-25°C (68°-77°F)

Avoid excessive heat above 40°C (104°F).

For Repackaging only.

DO NOT OPEN POUCHES UNTIL REPACKAGING

Mfd. by : Dr. Reddy's Laboratories Limited

Bachepalli - 502 325 INDIA.

Container:

Carton:

Pouch Label:

IBUPROFEN AND DIPHENHYDRAMINE CITRATE 
ibuprofen and diphenhydramine citrate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55111-565
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ibuprofen (ibuprofen) ibuprofen200 mg
diphenhydramine citrate (diphenhydramine) diphenhydramine38 mg
Inactive Ingredients
Ingredient NameStrength
carnauba wax 
STARCH, CORN 
colloidal silicon dioxide 
croscarmellose sodium 
FD&C blue no. 2 
CELLULOSE, MICROCRYSTALLINE 
HYPROMELLOSE 
polydextrose 
polyethylene glycol 400 
sodium lauryl sulfate 
stearic acid 
titanium dioxide 
Product Characteristics
ColorBLUE (blue) Scoreno score
ShapeCAPSULE (slightly glossy smooth blue film coated) Size15mm
FlavorImprint CodeRDY;565
Contains    
Packaging
#Item CodePackage Description
1NDC:55111-565-141 BOTTLE (1 BOTTLE) in 1 CARTON
120 TABLET (TABLET) in 1 BOTTLE
2NDC:55111-565-301 BOTTLE (1 BOTTLE) in 1 CARTON
230 TABLET (TABLET) in 1 BOTTLE
3NDC:55111-565-401 BOTTLE (1 BOTTLE) in 1 CARTON
340 TABLET (TABLET) in 1 BOTTLE
4NDC:55111-565-801 BOTTLE (1 BOTTLE) in 1 CARTON
480 TABLET (TABLET) in 1 BOTTLE
5NDC:55111-565-901 BOTTLE (1 BOTTLE) in 1 CARTON
590 TABLET (TABLET) in 1 BOTTLE
6NDC:55111-565-181 BOTTLE (1 BOTTLE) in 1 CARTON
6180 TABLET (TABLET) in 1 BOTTLE
7NDC:55111-565-051 BOTTLE (1 BOTTLE) in 1 CARTON
7500 TABLET (TABLET) in 1 BOTTLE
8NDC:55111-565-922500 TABLET (TABLET) in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09061901/31/2010
Labeler - Dr. Reddy's Laboratories Limited (862179079)

Revised: 11/2009
 
Dr. Reddy's Laboratories Limited

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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