Label: MUCUS RELIEF- antimony potassium tartrate, atropa belladonna, bryonia alba whole, anemone americana, hyoscyamus niger, ipecac, lobelia inflata, human sputum, bordetella pertussis infected, and lobaria pulmonaria tablet
- NDC Code(s): 62795-1012-2, 62795-1012-3
- Packager: MediNatura Inc
- 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 December 14, 2022
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- Uses:
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DIRECTIONS
At first sign of symptoms:
Adults and children 4 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage.
Standard dosage: Adults and children 4 years and older: Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours.
For children under 4, consult your health professional.
Allow tablets to dissolve completely in the mouth, do not swallow.
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- WARNINGS
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INGREDIENTS AND APPEARANCE
MUCUS RELIEF
antimony potassium tartrate, atropa belladonna, bryonia alba whole, anemone americana, hyoscyamus niger, ipecac, lobelia inflata, human sputum, bordetella pertussis infected, and lobaria pulmonaria tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-1012 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 5 [hp_X] ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 6 [hp_X] BRYONIA ALBA WHOLE (UNII: 56K0VVT47P) (BRYONIA ALBA WHOLE - UNII:56K0VVT47P) BRYONIA ALBA WHOLE 6 [hp_X] ANEMONE HEPATICA VAR. OBTUSA (UNII: 6ICN6T7FEM) (ANEMONE HEPATICA VAR. OBTUSA - UNII:6ICN6T7FEM) ANEMONE HEPATICA VAR. OBTUSA 6 [hp_X] HYOSCYAMUS NIGER (UNII: 4WRK2153H3) (HYOSCYAMUS NIGER - UNII:4WRK2153H3) HYOSCYAMUS NIGER 5 [hp_X] IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 6 [hp_X] LOBELIA INFLATA (UNII: 9PP1T3TC5U) (LOBELIA INFLATA - UNII:9PP1T3TC5U) LOBELIA INFLATA 4 [hp_X] HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - UNII:U364V64HUN) HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_X] LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T) LOBARIA PULMONARIA 5 [hp_X] Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) DEXTROSE (UNII: IY9XDZ35W2) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code Leafman Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62795-1012-3 1 in 1 CARTON 01/01/2015 1 100 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:62795-1012-2 100 in 1 BOTTLE; Type 0: Not a Combination Product 12/14/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2015 Labeler - MediNatura Inc (079324099) Establishment Name Address ID/FEI Business Operations MediNatura Inc 102783016 manufacture(62795-1012)