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Dosage form: tablet
Ingredients: GUAIFENESIN 200mg
Labeler: Enzymatic Therapy, Inc.
NDC Code: 59800-1232

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.


Guaifenesin 200 mg

Phytopharmica Brand
Dosage:  Adults and Children 12 years and over:
  1-2 tabs every 4 hours, not to exceed twelve tables in 24 hours.
Children 6 to 12 years of age: 1/2 to 1 tablets every four hours not to exceed 6 tablets in 24 hours.

Purpose: Helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of mucus and make coughs more productive.


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

Inactive Ingredients: Mullein Leaf Powder, Fenugreek Extract, PAPA (USP), Marshamallow Extract 3.5:1, Microcrystalline Cellulose

Pregnant or breast feeding warning:

If pregnant or breast feeding, ask a health professional before use.

Warnings:  Ask a doctor before use if you have:
     Persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
     cough that is accompanied by excessive phlegm (mucus).

Stop use and ask a doctor if cough persists more than one week, tends to recur, or is accompanied by a fever, rash or persisient headache.  A persistent cough may be a sign of a serious condition.

Warning for Children:

Keep out of the reach or Children


guaifenesin tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59800-1232
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Product Characteristics
Colorbrown (light brown to gray-brown w/ light and/or dark specks) Scoreno score
ShapeOVAL (Convex face, debossed 232 tablet) Size20mm
FlavorImprint Code232
#Item CodePackage Description
1NDC:59800-1232-1100 TABLET (TABLET) in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34105/19/2003
Labeler - Enzymatic Therapy, Inc. (056544166)
Enzymatic Therapy, Inc.056544166manufacture

Revised: 09/2010
Enzymatic Therapy, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.