Creosote Combination
Creosote Combination is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Creosote Combination 9254. Available dosage form: liquid.
Drug Details
- Generic Name
- Creosote Combination
- Brand Names
- Creosote Combination 9254
- Application Number
- Sponsor
- Professional Complementary Health Formulas
- NDC Codes
- 1
- Dosage Forms
- LIQUID
- Routes
- ORAL
- Active Ingredients
- ACONITUM NAPELLUS WHOLE, AMARYLLIS BELLADONNA WHOLE, BRYONIA ALBA ROOT, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA WHOLE, LOBARIA PULMONARIA, PHOSPHORUS, ANTIMONY POTASSIUM TARTRATE, WOOD CREOSOTE, SILICON DIOXIDE, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
Indications and Usage
INDICATIONS For the temporary relief of coughing, wheezing, chills, sweats, fatigue, minor aches and pains, and irritation, tenderness or mild pain in the nose or throat.*
Warnings
WARNINGS If symptoms do not improve or are accompanied by fever, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.