Label: CIMICIFUGA HOMACCORD - black cohosh and strontium carbonate and liquid
- NDC Code(s): 50114-1220-4
- Packager: Heel 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.
Updated February 28, 2012
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- KEEP OUT OF REACH OF CHILDREN
Keep this and all medicines out of the reach of children. Close
- INDICATIONS AND USAGE
For the temporary relief of:
- Headache rising from the neck
- Rheumatic pain in the neck, shoulders and back
- Sciatic neuralgia
If symptoms persist or worsen, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product. Close
- DOSAGE AND ADMINISTRATION
Adults and children above 11 years: 10 drops orally, 3 times daily, or as directed by a physician. Consult a physician for use in children under 12 years of age. Close
- ACTIVE INGREDIENT
Each 50 ml contains as active ingredients: Cimicifuga racemosa 2X, 10X, 30X, 200X 0.4 ml each; Strontium carbonicum 8X, 30X, 200X 0.1 ml each.
- INACTIVE INGREDIENT
Inactive ingredients: Ethanol, Purified Water USP.
Headache rising from the neck, Rheumatic pain in the neck, shoulders and back, Sciatic neuralgia
- INGREDIENTS AND APPEARANCE
black cohosh and strontium carbonate and liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50114-1220 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9) BLACK COHOSH 2 [hp_X] in 50 mL STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (CARBONATE ION - UNII:7UJQ5OPE7D) STRONTIUM CARBONATE 8 [hp_X] in 50 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50114-1220-4 50 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/31/1986 Labeler - Heel Inc (102783016) Establishment Name Address ID/FEI Business Operations Heel Inc 102783016 manufacture