Label: BACH ORIGINAL FLOWER REMEDIES- larix decidua whole solution
- NDC Code(s): 57687-268-20
- Packager: Nelson Bach USA Limited
- 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 June 2, 2020
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- Indications
- Directions
- Warnings
- Active Ingredients
- Inactive Ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 20 mL Bottle Label
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INGREDIENTS AND APPEARANCE
BACH ORIGINAL FLOWER REMEDIES
larix decidua whole solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57687-268 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Larix decidua whole (UNII: O8554H2U9W) (Larix decidua whole - UNII:O8554H2U9W) Larix decidua whole 5 [hp_X] in 0.095 mL Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57687-268-20 20 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 01/01/2002 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 01/01/2002 Labeler - Nelson Bach USA Limited (877720193) Registrant - A. Nelson & Co. Limited (221471234) Establishment Name Address ID/FEI Business Operations A. Nelson & Co Ltd 221471234 MANUFACTURE(57687-268) , PACK(57687-268) , LABEL(57687-268) , ANALYSIS(57687-268)