CAPRON DM- dextromethorphan hbr and pyrilamine maleate liquid

Capron DM by

Drug Labeling and Warnings

Capron DM by is a Otc medication manufactured, distributed, or labeled by Capital Pharmaceutical, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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 29978-127-15
Capron DM
Liquid
Candy Apple Flavor
1 5 mL

INGREDIENTS AND APPEARANCE

CAPRON DM 
dextromethorphan hbr and pyrilamine maleate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29978-127
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	7.5 mg  in 5 mL
PYRILAMINE MALEATE (UNII: R35D29L3ZA) (PYRILAMINE - UNII:HPE317O9TL)	PYRILAMINE MALEATE	7.5 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
METHYLPARABEN (UNII: A2I8C7HI9T)
POTASSIUM CITRATE (UNII: EE90ONI6FF)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color		Score
Shape		Size
Flavor	APPLE (Candy Apple)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29978-127-15	6 in 1 BOX	06/20/2013
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 29978-127-16	1 in 1 BOX	06/20/2013
2		473 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	06/20/2013

Labeler - Capital Pharmaceutical, LLC (831545541)