Label: BRONCHIAL COUGH THERAPY- antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, unspecified - calcium sulfide - human sputum, bordetella pertussis infected - spongia officinalis skeleton, roasted - tablet, orally disintegrating
- NDC Code(s): 17312-018-14
- Packager: TRP Company
- 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 April 4, 2024
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ACTIVE INGREDIENT
Active Ingredients Purpose Antimonium tartaricum HPUS 6c, 12c, 18c Rattling cough Coccus cacti HPUS 6c, 12c, 18c Congestive cough Drosera HPUS 6c, 12c, 18c Dry tickling cough Echinacea HPUS 6c, 12c, 18c Immune system support Hepar sulphuris calcareum HPUS 6c, 12c, 18c Expectorant Pertussinum HPUS 18c Recurring and Spasmodic coughing attacks Spongia tosta HPUS 6c, 12c, 18c Dry barking cough The letters HPUS indicate that the components of this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
- PURPOSE
- Uses
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Warnings
USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN.
- This product is a not a fast acting (rescue) inhaler.
- This product is intended to complement, not replace, standard medical treatment.
- Initial worsening of symptoms may occur.
- A physician should always be consulted to rule out serious causes.
- In case of overdose, get medical help or contact a Poison Control Center right away.
Stop use and ask a doctor if:
- You experience worsening symptoms.
- If symptoms last longer than 7 days.
- Keep out of reach of children
- PREGNANCY OR BREAST FEEDING
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Directions
- Suitable for adults and children 12 years and above.
- Dissolve entire tablet under tongue.
- Do not chew or swallow whole.
- Take 1 tablet 3 times a day or as directed by a physician.
- Use up to 6 times a day as needed.
- Take at least 10 minutes before or at least 10 minutes after eating or drinking.
- Children under the age of 12: consult a physician before use.
- Other information
- Inactive Ingredients
- Do not use if tamper evident seal is torn, broken or missing.
- QUESTIONS
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
BRONCHIAL COUGH THERAPY
antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, unspecified - calcium sulfide - human sputum, bordetella pertussis infected - spongia officinalis skeleton, roasted - tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-018 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 6 [hp_C] ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 6 [hp_C] PROTORTONIA CACTI (UNII: LZB7TFX1LT) (PROTORTONIA CACTI - UNII:LZB7TFX1LT) PROTORTONIA CACTI 6 [hp_C] DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA 6 [hp_C] ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX) ECHINACEA, UNSPECIFIED 6 [hp_C] CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 6 [hp_C] HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - UNII:U364V64HUN) HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 18 [hp_C] Inactive Ingredients Ingredient Name Strength MANNITOL (UNII: 3OWL53L36A) SORBITOL (UNII: 506T60A25R) CROSPOVIDONE (UNII: 2S7830E561) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) COPOVIDONE (UNII: D9C330MD8B) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white Score no score Shape DIAMOND Size 13mm Flavor Imprint Code TRP Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17312-018-14 1 in 1 PACKAGE 12/01/2011 1 70 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/01/2011 Labeler - TRP Company (105185719) Registrant - TRP Company (105185719)