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ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE

Dosage form: tablet, film coated
Ingredients: ACETAMINOPHEN 500mg, DIPHENHYDRAMINE HYDROCHLORIDE 25mg
Labeler: HIMPRIT PHARMACHEM PVT LTD
NDC Code: 65437-041

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.

ACETAINOPHEN AND DIPHENHYDRAMINE HCL TABLETS 500/25 mg

Drug Facts

Active ingredients (in each Caplet)Purpose
Acetaminophen 500 mgPain reliever/ fever reducer
Diphenhydramine HCL 25 mgSleep Aid

Uses

Temporary relief of occasional headaches and minor aches and pain with accompanying sleeplessness

Warnings

Alcohol Warnings

If you consume 3 or more alcoholic drinks every day, ask your doctor if you should take acetaminophen or other pain relievers/fever reducers. Acetaminophen may cause liver damage.

Do not use
*
with any other product containing acetaminophen
*
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

*
a breathing problem such as emphysema or chronic bronchitis
*
glaucoma
*
difficulty in urination due to enlargement of the prostate gland

ASK a doctor or pharmacists before use if you are taking sedatives or tranquilizers

When using this product

*
do not exceed recommended dosage
*
avoid alcoholic beverages
*
marked drowsiness may occur
*
do not drive a motor vehicle or operate machinery

Stop use and ask a doctor if

*
sleeplessness persists continuously for more than two weeks. Insomnia may be a symptom of a serious underlying medical illness
*
new symptoms occur
*
redness or swelling is present
*
pain gets worse or lasts more than 10 days
*
fever gets worse or lasts more than 3 days

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

Keep out of reach of children. In case of accidental overdose get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Direction
*
use as directed
*
adults and children 12 years and over : take 2 caplets at bedtime or as directed by a doctor
*
Children under 12 years : do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and could cause serious health problems.

Other information
*
Store at room temperature

Inactive ingredients

croscarmellose sodium, hypromellose, polythlene glycol,sodium metabisulfate, stearic acid,, sodium starch glycolate,collodial silicon dioxide, FD & C blue # 1

PRINCIPAL DISPLAY PANEL 500/25 mg Shipper Label

ACETAMINOPHEN AND DIPHENHYDRAMINE HCL TABLETS
Each Film coated Tablet Contains:

ACETAMEINOPHEN 500 mg
DIPHENHYDRAMINE HCL 25 mg

Lot No :
MFG. DATE :
Exp. Date :
Jar No. :
Quantity : 31000 Tablets
NDC. No : 65437-041-31

WARNING :
KEEP OUT OF THE REACH OF CHILDREN

STORE CONTROLLED ROOM TEMPRATURE OF 59° –86°F (15° – 30°C)
PROTECT FROM LIGHT, MOISTURE AND FREEZING

THIS IS A BULK SHIPMENT INTENDED FOR FURTHER PROCESSING ONLY.
CONTENTS SHOULD BE APPROVED,REPACKAGED IMMEDIATELY AND LABELED IN STRICT
CONFORMANCE WITH THE FDA AND REGULATIONS THEREUNDER

MANUFACTURED BY:
MANUFACTURED CODE No Guj/Drugs/G/1362
LABELER CODE # 14803

MANUFACTURED FOR:
HIMPRIT PHARMACHEM PVT. LTD

"LAKULISH", R.V.DESAI ROAD,
NEXT TO NAVAPURA POLICE STATION
BARODA, INDIA – 390 001

CAUTION : "FOR MANUFACTURING, PROCESSING OR REPACKING"

ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE 
acetaminophen and diphenhydramine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65437-041
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN500 mg
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM METABISULFITE 
CELLULOSE, MICROCRYSTALLINE 
CROSCARMELLOSE SODIUM 
STEARIC ACID 
POLYETHYLENE GLYCOL 
FD&C BLUE NO. 1 
TITANIUM DIOXIDE 
WATER 
SILICON DIOXIDE 
FD&C BLUE NO. 2 
HYPROMELLOSE 
TALC 
Product Characteristics
ColorBLUEScoreno score
ShapeOVAL (Capsule Shaped) Size18mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:65437-041-311 BAG (BAG) in 1 DRUM
131000 TABLET, FILM COATED (TABLET) in 1 BAG
2NDC:65437-041-501 BAG (BAG) in 1 DRUM
250000 TABLET, FILM COATED (TABLET) in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34307/01/2010
Labeler - HIMPRIT PHARMACHEM PVT LTD (917261992)

 
HIMPRIT PHARMACHEM PVT LTD

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Medically reviewed on Jun 15, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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