Country: Amerika Syarikat
Bahasa: Inggeris
Sumber: NLM (National Library of Medicine)
Kali bichromicum 6X, 9X, 12X, 30X
Professional Complementary Health Formulas
ORAL
OTC DRUG
Use according to standard homeopathic indications for self-limiting conditions. Common Materia Medica indications: excessive mucus, sinus congestion, nausea, vomiting.* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
unapproved homeopathic
KALI BICHROMICUM 7123- KALI BICHROMICUM LIQUID PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS _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._ ---------- DKAL ACTIVE INGREDIENTS Kali bichromicum 6X, 9X, 12X, 30X QUESTIONS Professional Formulas PO Box 2034 Lake Oswego, OR 97035 INDICATIONS Use according to standard homeopathic indications for self-limiting conditions. Common Materia Medica indications: excessive mucus, sinus congestion, nausea, vomiting.* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. WARNINGS In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use. DIRECTIONS Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age. OTHER INFORMATION Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat. INACTIVE INGREDIENTS 20% ethanol, purified water. LABEL Est 1985 Professional Formulas Complementary Health Kali bichromicum Homeopathic Remedy 1 FL. OZ. (29.5 mL) KALI BICHROMICUM 7123 kali bichromicum liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:63083-7123 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 6 [hp_X] in 29.5 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH ALCOHOL (UNII: 3K9958V90M) Professional Complementary Health Formulas WATER (UNII: 059QF0KO0R) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:63083- 7123-1 29.5 mL in 1 BOTTLE, DROP Baca dokumen lengkap