Yeast Gard Advanced

Yeast Gard Advanced is an FDA-registered drug product whose active ingredient is BERBERIS VULGARIS, BORAX, COLLINSONIA CANADENSIS, HAMAMELIS VIRGINIANA. It is labelled by Wisconsin Pharmacal Company taken by vaginal and marketed as a human otc drug product. Identifiers on file: NDC 68093-0668, label effective 20181206. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing BERBERIS VULGARIS, BORAX, COLLINSONIA CANADENSIS, HAMAMELIS VIRGINIANA are most often described in connection with: temporary relief, symptoms associated, vagianl yeast, infection including, itching burning. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Uses For the temporary relief of symptoms associated with vagianl yeast infection, including: itching burning irritation

Directions Directions Tamper Evident: If the foil seal on bottle opening is missing, torn or damaged in any way, do not use. Wash hands thoroughly with soap and water before and after use remove cap and safety seal from bottle. Carefully open teh packet and pour homeopathic contents into the douche bottle. Screw cap back onto bottle and shake thoroughly to fully mix powder into solution. After fully mixed, remove cap. Remove sanitary wrap from nozzle. Screw nozzle onto douche bottle. Slowly insert nozzle into vagina about 3 inches. If needed, a small amount of personal lubricant can be applied to nozzle to ease insertion of nozzle into vagina. Gently squeeze bottle until solution is dispensed. Use while sittion on the toilet, standing in the shower or in the tub. After douching discard bottle and nozzle.

Warnings Use only as directed For vaginal use only 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 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 vagina. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. Keep out of reach of children. If swallowed, get medial help or contact a Poison Control Center right away Do not use if you have never had a vaginal yeast infection diagnosed by a doctor When using this product if you do not get complete relief ask a doctor before using another product

3 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Yeast Gard Advanced used for?
Uses Uses For the temporary relief of symptoms associated with vagianl yeast infection, including: itching burning irritation

Who makes Yeast Gard Advanced?
Wisconsin Pharmacal Company is the labeler of record for Yeast Gard Advanced.

What form does Yeast Gard Advanced come in?
administered by vaginal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Yeast Gard Advanced prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Yeast Gard Advanced been recalled?
3 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.