Label: CANDIDA YEAST RELIEF- baptisia tinctoria, bryonia alba, echinacea angustifolia, thuja occidentalis, viscum album, candida albicans pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 60512-0017-1 - Packager: HOMEOLAB USA 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 January 22, 2020
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- ACTIVE INGREDIENTS HPUS
- REFERENCES
- PURPOSE
- USES
- WARNINGS
- ASK DOCTOR
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- Package Labeling:
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INGREDIENTS AND APPEARANCE
CANDIDA YEAST RELIEF
baptisia tinctoria, bryonia alba, echinacea angustifolia, thuja occidentalis, viscum album, candida albicans pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-0017 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT 4 [hp_X] BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 4 [hp_X] ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA 4 [hp_X] THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 4 [hp_X] VISCUM ALBUM WHOLE (UNII: E6839Q6DO1) (VISCUM ALBUM WHOLE - UNII:E6839Q6DO1) VISCUM ALBUM WHOLE 4 [hp_X] CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 14 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60512-0017-1 80 in 1 TUBE; Type 0: Not a Combination Product 10/18/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/18/2013 Labeler - HOMEOLAB USA INC. (202032533) Establishment Name Address ID/FEI Business Operations HOMEOLAB USA INC. 202032533 manufacture(60512-0017)