Label: YEAST GARD ADVANCED- borax, collinsonia canadensis, berberis vulgaris, hamamelis virginiana suppository
- NDC Code(s): 68093-7106-1
- Packager: Wisconsin Pharmacal Company
- 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 December 6, 2018
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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Warnings
For vaginal use only. Use only as directed.
Do not use if you have never had a vaginal yeast infection diagnosed by a doctor.
Stop use and ask a doctor if:
- Symptoms last more than 7 days
- You get a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Ask a doctor before use if you have
- Vaginal itching and discomfort for the first time
- Lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge. You may have a serious condition.
- Vaginal yeast infections often (such as once a month or 3 in 6 months). You could be pregnant or have a serious underlying medical cause for you symptoms, including diabetes or a weakened immune system.
- Been exposed to the human immunodeficiency virus (HIV) that causes AIDS
- You have an STD (sexually transmitted disease) or PID (Pelvic inflammatory disease)
- You have frequent and painful urination
- Directions
- Other information
- Inactive Ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YEAST GARD ADVANCED
borax, collinsonia canadensis, berberis vulgaris, hamamelis virginiana suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68093-7106 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 6 [hp_X] SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22) SODIUM BORATE 3 [hp_X] COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (COLLINSONIA CANADENSIS ROOT - UNII:O2630F3XDR) COLLINSONIA CANADENSIS ROOT 3 [hp_X] HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 6 [hp_X] Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) BACILLUS COAGULANS (UNII: ISK1LOY57E) POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68093-7106-1 10 in 1 CARTON 05/01/2008 1 1 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/01/2008 Labeler - Wisconsin Pharmacal Company (800873986) Establishment Name Address ID/FEI Business Operations Wisconsin Pharmacal Company 800873986 manufacture(68093-7106)