Get Expert Advice for controlling your Severe Allergies

Chlorpheniramine Tablets

Pronunciation

Generic Name: chlorpheniramine maleate
Dosage Form: tablet

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.

Chlorpheniramine maleate

ACTIVE INGREDIENT (IN EACH TABLET)

Chlorpheniramine Maleate 4 mg

Slideshow: 2014 Update - First Time Brand-to-Generic Switches

PURPOSE

Antihistamine

USES

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: ■ sneezing ■ runny nose ■ itchy, watery eyes ■ itching of the nose or throat

Warnings

Ask a doctor before use if you have

■ a breathing problem such as emphysema or chronic bronchitis, ■ glaucoma or ■ 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 product

■ marked drowsiness may occur ■ avoid alcoholic beverages ■ alcohol, sedatives, and tranquilizers may increase drowsiness ■ be careful when driving a motor vehicle or operating machinery ■ excitability may occur especially in children

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of accidental overdose, contact a doctor or Poison Control Center immediately.

Directions

■ take every 4 to 6 hours ■ do not take more than 6 doses in 24 hours ■ adults and children 12 years and over: 1 tablet ■ children 6 to under 12 years: 1/2 tablet ■ children under 6 years: consult a doctor

Other information

■ save carton for full directions and warnings ■ store at room temperature ■ do not use if imprinted safety seal under cap is broken or missing

Inactive ingredients

D.&C. Yellow #10 lake, lactose, magnesium stearate, microcrystalline cellulose, stearic acid. May contain starch.

DISPLAY PANEL

CHLORPHENIRAMINE MALEATE 
chlorpheniramine maleate tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62211-246
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLORPHENIRAMINE MALEATE (CHLORPHENIRAMINE) CHLORPHENIRAMINE MALEATE 4 mg
Inactive Ingredients
Ingredient Name Strength
STEARIC ACID  
LACTOSE  
STARCH, CORN  
MAGNESIUM STEARATE  
D&C YELLOW NO. 10  
CELLULOSE, MICROCRYSTALLINE  
Product Characteristics
Color yellow Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code AZ246
Contains         
Packaging
# Item Code Package Description
1 NDC:62211-246-93 24 TABLET (TABLET) in 1 PACKAGE
2 NDC:62211-246-99 75000 TABLET (TABLET) in 1 CARTON
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 02/12/2010
Labeler - A&Z Pharmaceutical, Inc. (926820705)
Registrant - A&Z Pharmaceutical, Inc. (926820705)
Revised: 10/2010
 
A&Z Pharmaceutical, Inc.



Hide
(web1)