Pyril DM description, usages, side effects, indications, overdosage, supplying and lots more!

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Pyril DM

Macoven Pharmaceuticals

PYRIL DM


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients (in each 5 mL) Purpose
Pyrilamine Maleate 16 mg Antihistamine
Phenylephrine HCl 5 mg Nasal Decongestant
Dextromethorphan HBr 15 mg Cough Suppressant

Pyril DM Uses

temporarily relieves

  • runny nose
  • sneezing
  • itching of the nose or throat
  • itchy, watery eyes due to hay fever or other upper respiratory allergies
  • nasal congestion due to the common cold
  • cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
  • the impulse to cough to help you get to sleep

Warnings

  • May cause excitability, especially in children

Do Not Use

  • 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.

Ask a doctor before use if you have

  • heart disease
  • diabetes
  • thyroid disease
  • high blood pressure
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • persistent or chronic cough such as occurs with emphysema, chronic bronchitis, or asthma
  • cough that occurs with too much phlegm (mucus)

Ask a doctor or pharmacist before use

  • If you or your child are taking sedatives or tranquilizers

When using this product

  • Do not exceed recommended dosage.
  • drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occurs
  • if symptoms do not improve within 7 days or are accompanied by a fever, rash, or headache. These could be signs of a serious condition.

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. 800-222-1222

Directions

  • take every 6 to 8 hours
  • do not take more than 4 doses in 24 hours or as directed by a doctor
Adults and children 12 years of age and older 1 to 2 teaspoonsful
Children 6 to under 12 years of age 1 teaspoonful
Children under 6 years of age Ask a doctor

Other Information

store at controlled room temperature 20°-25°C (68°-77°F)

  • Tamper Evident: Do not use if seal is broken or missing.

Inactive ingredients

Citric acid, FD&C Blue No. 1, FD&C Red No. 40, glycerin, grape flavor, magnesium aluminum silicate, methylparaben, purified water, sucralose, monoammonium glycyrrhizinate, sodium benzoate, sodium citrate dihydrate, sucrose, xanthan gum and galloquinate.

Questions?

Call 1-877-622-6836

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

MACOVEN
PHARMACEUTICALS, LLC

NDC 44183-210-16

PYRIL DM
SUSPENSION

Shake Well

Each 5 mL (one teaspoonful)
for oral administration contains:

Pyrilamine Maleate 16 mg
Phenylephrine HCl 5 mg
Dextromethorphan HBr 15 mg

GRAPE FLAVOR

16 fl. oz. (473 mL)

Pyril DM

Pyril DM

PHENYLEPHRINE HYDROCHLORIDE, PYRILAMINE MALEATE, and DEXTROMETHORPHAN HYDROBROMIDE SUSPENSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44183-210
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Phenylephrine Hydrochloride PHENYLEPHRINE 5 mg
PYRILAMINE MALEATE PYRILAMINE 16 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 15 mg

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
FD&C BLUE NO. 1
FD&C RED NO. 40
GLYCERIN
GRAPE
magnesium aluminum silicate
METHYLPARABEN
water
Sucralose
GLYCYRRHIZIN, AMMONIATED
SODIUM BENZOATE
SODIUM CITRATE
SUCROSE
XANTHAN GUM
TANNIC ACID

Product Characteristics

Color
PURPLE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44183-210-16 473 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2011-02-01


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Be sure to consult your doctor before taking any medication!
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