Diabetic Siltussin DAS-Na description, usages, side effects, indications, overdosage, supplying and lots more!

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Diabetic Siltussin DAS-Na

Preferred Pharmaceuticals Inc.

Diabetic Siltussin DAS-Na


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

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

Purpose

Purpose: Expectorant

Uses

Uses

Helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.

Warnings

Ask a doctor before use if you have

  • •cough that occurs with too much phlegm (mucus)
  • •cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

Stop use and ask a doctor if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent 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.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

  • •do not take more than 6 doses in any 24-hour period repeat dose every 4 hours

Adult and children 12 years and over

2 teaspoonfuls

Children under 12 years

DO NOT USE

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

Phenylketonurics: contains phenylalanine 3 mg per teaspoonful (5 mL)

Inactive Ingredients

Acesulfame-K, aspartame, benzoic acid, citric acid, hydroxypropyl methyl cellulose, methylparaben, propylene glycol, strawberry flavor, and water.

How Supplied

118cc Bottle - 68788-6759-1

Questions

888-974-5279

* This product is not manufactured or distributed by Wyeth Consumer Healthcare, distributor of Robitussin®

Manufactured by:

Silarx Pharmaceuticals, Inc.
19 West Street,
Spring Valley, NY 10977
USA

Relabeled by Preferred Pharmaceuticals, Inc.

Diabetic Siltussin DAS-Na

Guaifenesin LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68788-6759(NDC:54838-138)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Guaifenesin GUAIFENESIN 100 mg

Inactive Ingredients

Ingredient Name Strength
ACESULFAME POTASSIUM
ASPARTAME
BENZOIC ACID
ANHYDROUS CITRIC ACID
HYPROMELLOSE 2910 (4000 MPA.S)
METHYLPARABEN
propylene glycol
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68788-6759-1 118 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2012-07-26


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