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Name:Tussin Original
Manufacturer:Aaron Industries, Inc.
Category:Over-the-counter (OTC) Marketed Drugs


Drug Facts

TUSSIN ORIGINAL  - guaifenesin liquid 
Aaron Industries, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients

Guaifenesin, USP 100 mg

Purpose

Expectorant

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

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

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Tussin

Compare to the active ingredient in Robitussin

Chest Congestion formula

Expectorant Guaifenesin Syrup, USP
For Adults

4 fl oz 188 mL

image of label


TUSSIN ORIGINAL 
robitussin liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49580-0413
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 100 mg  in 5 mL
Inactive Ingredients
Ingredient Name Strength
DEXTROSE  
GLYCERIN  
HIGH FRUCTOSE CORN SYRUP  
MENTHOL  
SACCHARIN SODIUM  
SODIUM BENZOATE  
Product Characteristics
Color red (red 40) Score     
Shape Size
Flavor CARAMEL (caramel) , CHERRY (cherry) Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49580-0413-4 118 mL in 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 01/16/2009

Labeler - Aaron Industries, Inc. (101896231)
Registrant - Aaron Industries, Inc. (101896231)
Establishment
Name Address ID/FEI Operations
Aaron Industries, Inc. 101896231 manufacture, analysis

Revised: 11/2009 Aaron Industries, Inc.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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