Label: BOBA HOMO- babesia microti, borrelia burgdorferi nosode liquid
- NDC Code(s): 43742-1716-1
- Packager: Deseret Biologicals, 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.
Drug Label Information
Updated February 20, 2024
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- ACTIVE INGREDIENTS:
- PURPOSE:
- USES:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
BOBA HOMO
babesia microti, borrelia burgdorferi nosode liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-1716 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BABESIA MICROTI (UNII: 1948X6KEG3) (BABESIA MICROTI - UNII:1948X6KEG3) BABESIA MICROTI 15 [hp_X] in 1 mL BORRELIA BURGDORFERI (UNII: 0J8NV9V5Q8) (BORRELIA BURGDORFERI - UNII:0J8NV9V5Q8) BORRELIA BURGDORFERI 15 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-1716-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 10/07/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/07/2020 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-1716) , api manufacture(43742-1716) , label(43742-1716) , pack(43742-1716)