Label: LEADER MUCUS ER- guaifenesin tablet, extended release
- NDC Code(s): 37205-628-58, 37205-628-60
- Packager: Cardinal Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Updated May 28, 2014
If you are a consumer or patient please visit this version.
- Active ingredient (in each extended-release tablet)
Guaifenesin 600 mgClose
helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productiveClose
Ask a doctor before use if you have
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
- cough accompanied by too much phlegm (mucus)
Stop use and ask a doctor if
- cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
- do not crush, chew, or break tablet
- take with a full glass of water
- this product can be administered without regard for the timing of meals
- adults and children 12 years of age and over: one or two tablets every 12 hours. Do not exceed 4 tablets in 24 hours.
- children under 12 years of age: do not use
- Other information
- do not use if printed seal under cap is broken or missing
- store between 20-25°C (68-77°F)
- Inactive ingredients
compressible sugar, copovidone, hydroxyethyl cellulose, silicon dioxide, zinc stearateClose
- Questions or comments?
- Package/Label Principal Display Panel
Compare to Mucinex® active ingredient
Guaifenesin Extended-Release Tablets, 600 mg
Relieves Chest Congestion
Thins and Loosens Mucus
20 EXTENDED-RELEASE TABLETS
- INGREDIENTS AND APPEARANCE
LEADER MUCUS ER
guaifenesin tablet, extended release
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37205-628 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg Inactive Ingredients Ingredient Name Strength COPOVIDONE K25-31 (UNII: D9C330MD8B) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ZINC STEARATE (UNII: H92E6QA4FV) Product Characteristics Color WHITE ((off-white)) Score no score Shape ROUND Size 12mm Flavor Imprint Code L498 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37205-628-58 1 in 1 CARTON 1 40 in 1 BOTTLE 2 NDC:37205-628-60 1 in 1 CARTON 2 20 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078912 03/19/2013 Labeler - Cardinal Health (097537435)