CAPRON DM- dextromethorphan hydrobromide and pyrilamine maleate liquid 
Capital Pharmaceutical, LLC

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.

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Capron DM Liquid

Drug Facts

Active Ingredients      

(in each 5 mL teaspoonful)

Dextromethorphan HBr 7.5 mg      

Purpose

Antitussive

Active Ingredients      

(in each 5 mL teaspoonful)

Pyrilamine Maleate 7.5 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies:

  • runny nose
  • sneezing
  • itching of the nose or throat
  • itchy, watery eyes
  • cough due to minor throat and bronchial irritation associated with a cold
  • alleviates cough to help you sleep
  • nonnarcotic cough suppressant for the relief of cough

Warnings

Do not exceed recommended dosage.

  • a persistent cough may be a sign of a serious condition. If cough persist for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache, consult a doctor.

Do not use this product

  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product
  • for persistent or chronic cough such as occurs with smoking, asthma, or emphysema, or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor

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 before use if you are taking

sedatives or tranquilizers.

When using this product

  • excitability may occur, especially in children
  • may cause marked drowsiness
  • sedatives and tranquilizers may increase drowsiness effect
  • avoid alcoholic beverages
  • use caution when driving a motor vehicle or operating machinery

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.

Directions

Do not exceed recommended dosage.

Adults and children 12 years of age and over:4 teaspoonfuls every 6-8 hours, not to exceed 16 teaspoonfuls in 24 hours, or as directed by a doctor
Children 6 to under 12 years of age:2 teaspoonfuls every 6-8 hours, not to exceed 8 teaspoonfuls in 24 hours, or as directed by a doctor
Children 2 to under 6 years of age
(For Professional Use Only)		1 teaspoonful every 6-8 hours, not to exceed 4 teaspoonfuls in 24 hours, or as directed by a doctor
Children under 2 years of age:Consult a doctor

Inactive ingredients

Citric Acid, Flavor, Magnasweet, Methyl Paraben, Potassium Citrate, Potassium Sorbate, Propyl Paraben, Propylene Glycol, Purified Water, Sorbitol, Sucralose

Questions or Comments?

Call 614.638.4622      

PRINCIPAL DISPLAY PANEL

NDC 29978-127-16
Capron DM
Liquid
Candy Apple Flavor
16 oz. (473 mL)

PRINCIPAL DISPLAY PANEL NDC 29978-127-16 Capron DM Liquid Candy Apple Flavor 16 oz. (473 mL)

CAPRON DM 
dextromethorphan hbr and pyrilamine maleate liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:29978-127
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE7.5 mg  in 5 mL
PYRILAMINE MALEATE (PYRILAMINE) PYRILAMINE MALEATE7.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
AMMONIUM GLYCYRRHIZATE 
METHYLPARABEN 
POTASSIUM CITRATE 
POTASSIUM SORBATE 
PROPYLPARABEN 
PROPYLENE GLYCOL 
WATER 
SORBITOL 
SUCRALOSE 
Product Characteristics
Color    Score    
ShapeSize
FlavorAPPLE (Candy Apple) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:29978-127-161 in 1 BOX
1473 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34106/20/2013
Labeler - Capital Pharmaceutical, LLC (831545541)

Revised: 7/2013
Document Id: b1a18263-f204-48f5-b08f-a19b2aab753f
Set id: cf778c5f-475e-4a86-a87c-2be1e665f5a5
Version: 1
Effective Time: 20130712
 
Capital Pharmaceutical, LLC