Label: YEASTAWAY- sodium borate, calendula officinalis flowering top, candida albicans, goldenseal suppository
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Contains inactivated NDC Code(s)
NDC Code(s): 0220-9375-62 - Packager: Laboratoires Boiron
- 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 July 20, 2020
If you are a consumer or patient please visit this version.
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Active Ingredients
Borax 14X HPUS (0.15g), Calendula officinalis 1X HPUS (0.15g), Candida Albicans 30X HPUS (0.15g), Hydrastis canadensis 5X HPUS (0.15g)
(In each suppository)
(contains less than 10 -3 mg hydrastine and berberine alkaloids)
The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
- Purpose
- Uses*
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Warnings
For vaginal use only.
Yeastaway may damage condoms and diaphragms and cause them to fail.
Ask a doctor before use if you
have one or more of the following:
Abdominal pain, fever, chills, nausea, vomiting, foul-smelling discharge.
Get vaginal yeast infections often (such as once a month or three in six months).
May have been exposed to the human immunodeficiency virus (HIV) that causes AIDS
Are under 12 years of age.When using this product
Do not use tampons, douche, spermicides
Do not have vaginal intercourse (sex). -
Directions
Before using Yeastaway, read the enclosed educational brochure for complete instructions and information.
Adults and children 12 years of age and older: Insert one suppository high into the vagina every night for 7 consecutive nights.
Applicator is included.
Children under 12 years of age: Ask a doctor - Other information
- SPL UNCLASSIFIED SECTION
- Inactive Ingredients
- Questions or comments?
- Principle Display Panel - Yeastaway suppository
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INGREDIENTS AND APPEARANCE
YEASTAWAY
sodium borate, calendula officinalis flowering top, candida albicans, goldenseal suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-9375 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X] CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 30 [hp_X] GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 5 [hp_X] SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22) SODIUM BORATE 14 [hp_X] Inactive Ingredients Ingredient Name Strength GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0220-9375-62 7 in 1 BOX; Type 0: Not a Combination Product 09/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2016 Labeler - Laboratoires Boiron (282560473) Registrant - Boiron Inc. (014892269) Establishment Name Address ID/FEI Business Operations Boiron 282560473 manufacture(0220-9375)