Tussin Original description, usages, side effects, indications, overdosage, supplying and lots more!

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Tussin Original

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Aaron Industries, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Guaifenesin, USP 100 mg

Purpose

Expectorant

Tussin Original 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

When using this product

do not use more than directed

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 this and all drugs out of the reach of children.

In case of accidental overdose, seek
professional assistance or contact a Poison
Control Center immediately.

Directions

do not exceed 6 doses in a 24-hour period
• this adult product is not intended for use in
children under 12 years of age



adults and children 12 years and over      2-4 teaspoonfuls (tsps) every 4 hours
      
children under 12 years do not use

Tussin Original Other information

store at controlled room temperature
• dosage cup provided
• alcohol-free

Inactive ingredients

caramel, citric acid, flavor, glucose, glycerin,
high fructose corn syrup, menthol, purified water,
red 40, saccharin sodium, sodium benzoate

principal display panel












Tussin Original

Tussin Original

GUAIFENESIN LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:15127-940
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
DEXTROSE
GLYCERIN
HIGH FRUCTOSE CORN SYRUP
MENTHOL
saccharin sodium
SODIUM BENZOATE
FD&C RED NO. 40

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:15127-940-48 237 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2009-06-17


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