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

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Siltussin DM

Preferred Pharmaceuticals, Inc

Siltussin DM Cough Syrup


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient: Guaifenesin 100 mg (in each 5 mL)

Active Ingredient: Dextromethorphan Hydrobromide 10 mg (in each 5 mL)

Purpose

Purpose of Guaifenesin: Expectorant

Purpose of Dextromethorphan Hydrobromide: Cough Suppressant

Uses

Uses

  • temporarily relieves cough due to minor throat and bronchial irritation
  • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Warnings


Do not use

Ask a doctor before use if you have

  • persistent cough or chronic cough such as occurs with smoking, asthma, chronic bronchitis, emphysema
  • cough accompanied by excessive phlegm (mucus)

Stop use and ask a doctor if

  • cough lasts more than 7 days or occurs with fever, rash, or headaches that lasts. This could be signs of a serious condition
  • hypersensitive to any ingredients

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.

Directions

This adult product is not intended for use in children under 12 years of age

Adults and children 12 years and over
2 teaspoonfuls (10 mL)
every 4 hours
Children under 12 years DO NOT USE

Inactive ingredients

citric acid, FD&C red no. 40, glycerin, menthol, methylparaben, propylene glycol, saccharin sodium, sodium benzoate, strawberry flavor, sucrose, purified water.

Siltussin DM Other information

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

Questions: 888-974-5279


Manufactured by

Silarx Pharmaceutical Inc,

19 West Street , Spring Valley

NY - 10977- USA.

Relabeled By:

Preferred Pharmaceuticals, Inc

Anaheim, CA 92807



Siltussin DM


Siltussin DM

Guaifenesin and Dextromethorphan Hydrobromide LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68788-9103(NDC:54838-209)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Guaifenesin GUAIFENESIN 100 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 10 mg

Inactive Ingredients

Ingredient Name Strength
Citric acid
FD&C RED NO. 40
GLYCERIN
MENTHOL
METHYLPARABEN
propylene glycol
saccharin sodium
SODIUM BENZOATE
SUCROSE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68788-9103-1 118 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 1992-09-05


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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