Label: ELP ESSENTIAL DM- dextromethorphan hydrobromide, guaifenesin syrup
- NDC Code(s): 70242-139-06
- Packager: Dannso Corp./d.b.a. Essential Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 27, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients: (in each 5 ml)
- Purpose
- Uses
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Warnings
Do not exceed recommended dosage.
Do not use
• If you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric 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 your doctor or pharmacist before taking this product.
• If you have a chronic pulmonary disease or shortness of breath unless directed by a doctor.
• Avoid alcoholic beverages while you taking this product.Ask the doctor before use if you have
• Cough that occurs with too much phlegm (mucus)
• Cough that last or is a chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema.Stop use and ask the doctor if
• Nervousness, dizziness or sleeplessness occurs.
• Cough persists for more than 1 week, tends to recur, or accompanied by fever, rash or persistent headache. A persistent cough may be sign serious conditionIf pregnant or breast-feeding, ask a health professional before use.
- Directions:
- Other Information
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Inactive Ingredients
Blue Cohosh, Citric Acid, Echinacea, Eucalyptus Oil, Ginkgo Biloba, Golden Seal Root, Honey Pure, Honey flavor, Horehound Herb, Licorice Root, Menthol, Mullein, Myrrh, Potassium Sorbate, Slippery Elm Bark, Sodium Benzoate, Propylene Glycol, Purified Water, Sodium Chloride, Sucralose, Wild Cherry bark and Zinc Sulfate.
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- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
ELP ESSENTIAL DM
dextromethorphan hydrobromide, guaifenesin syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70242-139 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg in 5 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg in 5 mL Inactive Ingredients Ingredient Name Strength CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) EUCALYPTUS OIL (UNII: 2R04ONI662) GINKGO (UNII: 19FUJ2C58T) GOLDENSEAL (UNII: ZW3Z11D0JV) HONEY (UNII: Y9H1V576FH) HOREHOUND (UNII: K08036XEJV) LICORICE (UNII: 61ZBX54883) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172) MYRRH (UNII: JC71GJ1F3L) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ULMUS RUBRA BARK (UNII: 91QY4PXU8Q) SODIUM BENZOATE (UNII: OJ245FE5EU) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SUCRALOSE (UNII: 96K6UQ3ZD4) PRUNUS SEROTINA BARK (UNII: 5D48E975HA) ZINC SULFATE, UNSPECIFIED FORM (UNII: 89DS0H96TB) Product Characteristics Color Score Shape Size Flavor HONEY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70242-139-06 1 in 1 BOX 10/26/2023 1 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 10/26/2023 Labeler - Dannso Corp./d.b.a. Essential Products (059741071)
