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

Menu
Search

Siltussin SA

Preferred Pharmaceuticals, Inc

Siltussin SA (Guaifenesin Liquid)


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.

Directions

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

adults and children 12 years and over
2-4 teaspoonfuls
children under 12 years DO NOT USE
Other information

Do not accept if imprinted tamperevident safety seal around cap is broken or missing

Inactive ingredients

citric acid, D&C yellow no. 10, FD&C blue no. 1, FD&C red no. 40, strawberry flavor, glycerin, propylene glycol, saccharin sodium, sodium benzoate, sodium citrate, sorbitol, purified water.

Questions

888-974-5279

† This product is not manufactured or distributed by Wyeth Consumer Healthcare, owner of the registered trademark Robitussin®.

Manufactured by:

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

Relabeled by:

Preferred Pharmaceuticals, Inc.
1Anaheim, CA 92807


Siltussin SA


Siltussin SA

Guaifenesin LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68788-9098(NDC:54838-117)
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
ANHYDROUS CITRIC ACID
D&C YELLOW NO. 10
FD&C BLUE NO. 1
FD&C RED NO. 40
GLYCERIN
propylene glycol
saccharin sodium
SODIUM BENZOATE
SODIUM CITRATE
sorbitol
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68788-9098-1 118 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 1998-10-05


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.