Label: AQUAFLORA PHASE II- candida albicans liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 57955-1602-6 - Packager: King Bio 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 April 3, 2018
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- HPUS Active Ingredients
- Uses
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- Directions
- Purpose
- Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AQUAFLORA PHASE II
candida albicans liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57955-1602 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 6 [hp_C] in 473 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARYA OVATA BARK (UNII: X765CF609L) CITRUS BIOFLAVONOIDS (UNII: BD70459I50) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) POLYEPSILON-LYSINE (4000 MW) (UNII: WB0M8X4TWR) REBAUDIOSIDE A (UNII: B3FUD0528F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57955-1602-6 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/03/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/03/2018 Labeler - King Bio Inc (617901350) Registrant - King Bio Inc (617901350) Establishment Name Address ID/FEI Business Operations King Bio Inc 617901350 manufacture(57955-1602)