Label: CODITUSSIN DAC- codeine phosphate, guaifenesin, and pseudoephedrine hydrochloride syrup
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Contains inactivated NDC Code(s)
NDC Code(s): 70147-414-16 - Packager: Glendale Inc
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated May 10, 2016
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- ACTIVE INGREDIENT
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Uses
temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:
- cough due to minor throat and bronchial irritation
- helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive
- reduces swelling of nasal passages
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Warnings
Do not exceed recommended dosage.
Do not use this product
- if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor before use if you have
- a cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema
- a cough that occurs with too much phlegm (mucus)
- chronic pulmonary disease or shortness of breath, or children who are taking other drugs
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- trouble urinating due to an enlarged prostate gland
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Directions
Do not exceed recommended dosage.
Adults and children 12 years of age and over: 2 teaspoonfuls every 4 to 6 hours, not to exceed 8 teaspoons in a 24 hour period Children 6 to under 12 years of age: 1 teaspoonfuls every 4 to 6 hours, not to exceed 8 teaspoons in a 24 hour period *Children under 6 years of age: Consult a doctor A special measuring device should be used to give an accurate dose of this product to children under 6 years of age. Giving a higher dose than recommended by a doctor could result in serious side effects for your child.
- Other information
- Inactive ingredients
- Questions? Comments?
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PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
NDC 70147-414-16
Coditussin
DACExpectorant
Cough Suppressant
Nasal DecongestantCV
Each teaspoonful for oral
administration contains:Codeine Phosphate* 10 mg
*(Warning: May be habit-forming)Guaifenesin 200 mg
Pseudoephedrine HCl 30 mg
SUGAR FREE / DYE FREE
ALCOHOL FREE / GLUTEN FREEGrape Flavored Liquid
Tamper evident by foil seal under cap.
Do not use if foil seal is broken or missing.Distributed by:
Glendale Inc
Villa Park, IL 60181
16 fl oz. (473 mL)
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INGREDIENTS AND APPEARANCE
CODITUSSIN DAC
codeine phosphate, guaifenesin, and pseudoephedrine hydrochloride syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70147-414 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CODEINE PHOSPHATE (UNII: GSL05Y1MN6) (CODEINE ANHYDROUS - UNII:UX6OWY2V7J) CODEINE PHOSPHATE 10 mg in 5 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 5 mL PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 30 mg in 5 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) Product Characteristics Color Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70147-414-16 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part341 05/01/2016 Labeler - Glendale Inc (079987961)