Label: COUGH AND MUCUS GRAPE FLAVOR- antimony potassium tartrate,bryonia alba root,ferrosoferric phosphate,calcium sulfide,ipecac,phosphorus,anemone pulsatilla,rumex crispus root liquid
- NDC Code(s): 54973-4056-1, 54973-4056-3
- Packager: Hyland's
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated October 29, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PURPOSE
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Drug Facts
Active ingredients Purpose Antimonium Tartaricum 15X HPUS cough Bryonia Alba 15X HPUS sore throat, mucus in throat, cough Ferrum Phosphoricum 12X HPUS mucus in throat, cough Hepar Sulph Calc 12X HPUS mucus in chest, cough Ipecacuanha 12X HPUS cough, sore throat Phosphorus 15X HPUS runny nose, chest or nasal congestion Pulsatilla 12X HPUS mucus in chest or throat, cough, sneezing Rumex Crispus 6X HPUS runny nose, sneezing "HPUS" is the Homeopathic Pharmacopoeia of the United States.
- Uses
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Warnings
Sore throat warning
If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
Ask a doctor before use if you have
■ persistent or chronic cough such as smoking, asthma, chronic bronchitis or emphysema. A persistent cough may be a sign of a serious condition. ■ cough that is accompanied by excessive phlegm (mucus).
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Directions
■ Use as directed. ■ Do not refrigerate. ■ Shake well before using. ■ Measure only with the dosing cup provided. ■ Do not use dosing cup with other products. ■ On dosing cup, mL = millilite
Children 2 years to under 6 years 5 mL up to 6 times per day (every 4 hours). Children 6 years to under 12 years 10 mL up to 6 times per day (every 4 hours). Adults and children 12 years and over 15 mL up to 6 times per day (every 4 hours).
- Inactive ingredients
- Questions?
- *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
- DO NOT USE IF TAMPER-EVIDENT SEAL IS BROKEN OR MISSING.
- PACKAGE LABEL - 118 mL BOTTLE CARTON
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INGREDIENTS AND APPEARANCE
COUGH AND MUCUS GRAPE FLAVOR
antimony potassium tartrate,bryonia alba root,ferrosoferric phosphate,calcium sulfide,ipecac,phosphorus,anemone pulsatilla,rumex crispus root liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-4056 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 6 [hp_X] in 1 mL BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 15 [hp_X] in 1 mL ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) ANEMONE PULSATILLA 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 15 [hp_X] in 1 mL FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 12 [hp_X] in 1 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X] in 1 mL IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 12 [hp_X] in 1 mL ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 15 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) SODIUM BENZOATE (UNII: OJ245FE5EU) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Product Characteristics Color Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-4056-1 1 in 1 CARTON 03/01/2022 1 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:54973-4056-3 5 mL in 1 POUCH; Type 0: Not a Combination Product 10/29/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/01/2022 Labeler - Hyland's (008316655) Establishment Name Address ID/FEI Business Operations Hylands 008316655 manufacture(54973-4056) , pack(54973-4056) , label(54973-4056) Establishment Name Address ID/FEI Business Operations LGM Pharma Solutions, LLC 117549198 manufacture(54973-4056) , pack(54973-4056) , label(54973-4056)

