Label: BRONCOMAR EXPECTORANT SF- guaifenesin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70242-100-06 - Packager: Dannso Corp./d.b.a. Essential Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 January 1, 2016
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- ASK DOCTOR
- Ask a doctor before use
- Do not use
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
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Inactive Ingredient
Blue Cohosh, Citric Acid, Echinacea Oil, Ginkgo Biloba, Glycerin Seal Root, Honey Flavor, Horehound Herb, Licorice, Golden Seal Root, Menthol, Mullein, Myrrh, Potassium Sobate, Slippery Elm Bark, Sodium Benzoate, Propylene Glycol, Purifed Water, sodium Chloride, Sucralose, Wild Cheery bark, and Zinc Sulfate.
- Questions or Comments
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BRONCOMAR EXPECTORANT SF
guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70242-100 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 (UNII: 4N9P6CC1DX) EUCALYPTUS OIL (UNII: 2R04ONI662) GINKGO (UNII: 19FUJ2C58T) GLYCERIN (UNII: PDC6A3C0OX) GOLDENSEAL (UNII: ZW3Z11D0JV) HONEY (UNII: Y9H1V576FH) HOREHOUND (UNII: K08036XEJV) LICORICE (UNII: 61ZBX54883) MENTHOL (UNII: L7T10EIP3A) VERBASCUM THAPSUS (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 (UNII: 89DS0H96TB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70242-100-06 1 in 1 CARTON 01/01/2015 1 177 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 10/01/2001 Labeler - Dannso Corp./d.b.a. Essential Products (059741071) Registrant - Dannso Corp./d.b.a. Essential Products (059741071) Establishment Name Address ID/FEI Business Operations All Pharma LLC 078572520 MANUFACTURE(70242-100)