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ACTIDOGESIC

Medically reviewed by Drugs.com. Last updated on Nov 24, 2020.

Dosage form: tablet
Ingredients: DEXBROMPHENIRAMINE MALEATE 1mg, ACETAMINOPHEN 500mg
Labeler: ACTIPHARMA, INC
NDC Code: 63102-402

Drug Facts

Active Ingredients in each caplet:Dexbrompheniramine Maleate 1 mg, Acetaminophen 1mg

Antihistamine, Pain reliever/fever reducer

Uses

• For the temporary relief of minor aches and pains associated with • headache

• muscular aches • backaches • minor arthritis pain • common cold • toothaches • menstrual

cramps • temporarily reduces fever • itchy and watery eyes due to hay fever.

Warnings

Liver Warning:

This product contains acetaminophen. Severe liver damage may occur if you take • more than 8 caplets (4,000 mg) in 24 hours, which is the maximum daily amount • with other drugs containing acetaminophen • 3 or more alcoholic drinks every day while using this product

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include: • skin reddening • blisters • rash

Caution: May cause drowsiness; alcohol, sedatives, and tranquilizers may increase the

drowsiness effect. Avoid alcoholic beverages while taking this product. Use caution when

driving a motor vehicle or operating machinery. Do not take this product if you are taking

sedatives or tranquilizers, without first consulting your doctor.

Ask a doctor before use

• if you have liver disease • if you are taking the blood thinning drug warfarin.

Stop using this product and ask a doctor if

• pain gets worse or lasts more than 10 days • fever gets worse or lasts more than 3 days

• new symptoms occur • redness or swelling is present • These could be signs of a serious condition.

Do not use

• with any other drug containing acetaminophen (prescription or nonprescription) this will provide more than the recommended dose (overdose) of acetaminophen and could cause serious health concerns. If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist • if you are allergic to acetaminophen or any of the inactive ingredients in the product • for more than 10 days for pain, unless directed by a doctor.

Do not take this product, unless directed by a doctor, if you have a breathing problem such as emphysema or chronic bronchitis, if you have glaucoma or difficulty in urination due to enlargement of the prostate gland.

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 (1-800-222-1222). Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms

Directions • Do not exceed recommended dosage

Adults and children 12 years of age and older:

Take 2 caplets every 4 to 6 hours as needed, do not exceed 8 caplets in 24 hours, or as directed by a doctor, do not use for more than 10 days

unless directed by a doctor.

Children under 12 years of age:

Do not use.

Other Information

• Tamper Evident. Do not use if inner seal is torn, broken, or missing

• Store at controlled room temperature 15°- 30°C (59°- 86°F)

• Avoid excessive heat or humidity

Inactive Ingredients: FD&C Red #40, FD&C Yellow #6, hypromellose, microcrystalline cellulose, polyethylene glycol, povidone, sodium starch glycolate, starch, stearic acid, and titanium dioxide

ACTIDOGESIC 
dexbrompheniramine maleate, acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-402
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXBROMPHENIRAMINE MALEATE (DEXBROMPHENIRAMINE) DEXBROMPHENIRAMINE MALEATE1 mg
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 
FD&C YELLOW NO. 6 
HYPROMELLOSE, UNSPECIFIED 
MICROCRYSTALLINE CELLULOSE 
POLYETHYLENE GLYCOL, UNSPECIFIED 
POVIDONE, UNSPECIFIED 
SODIUM STARCH GLYCOLATE TYPE A CORN 
STARCH, CORN 
STEARIC ACID 
TITANIUM DIOXIDE 
Product Characteristics
ColororangeScore2 pieces
ShapecapsuleSize17mm
FlavorImprint CodeA402
Contains    
Packaging
#Item CodePackage Description
1NDC:63102-402-10100 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34110/14/2016
Labeler - ACTIPHARMA, INC (079340948)
Registrant - ACTIPHARMA, INC (079340948)

 
ACTIPHARMA, INC

Further information

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

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