Label: TOTAL ANTIMONY- antimonium tartaricum liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 61657-0966-1 - Packager: White Manufacturing Inc. DBA Micro -West
- Category: HUMAN OTC DRUG LABEL
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 20, 2016
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- Active Ingredients
- Uses
- Keep Out of Reach of Children
- INDICATIONS
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- Directions
- Inactive Ingredient
- SPL UNCLASSIFIED SECTION
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INGREDIENTS AND APPEARANCE
TOTAL ANTIMONY
antimonium tartaricum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61657-0966 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 12 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61657-0966-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 11/04/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/13/2011 Labeler - White Manufacturing Inc. DBA Micro -West (082307831) Establishment Name Address ID/FEI Business Operations King Bio 617901350 manufacture(61657-0966) , pack(61657-0966) , label(61657-0966)