FDA.reportPublic FDA data

Yeast Gard Advanced

Manufacturer
Wisconsin Pharmacal Company
Effective date
2018-12-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:10:34

Label at a glance#

ProductYeast Gard Advanced
Active ingredientBERBERIS VULGARIS ROOT BARK, SODIUM BORATE, COLLINSONIA CANADENSIS ROOT, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
Label structure8 sections

Dosage and administration

Remove one suppository from the foil wrap and place in the applicator.  Insert suppository into the vagina with the applicator.  Remove applicator and cleanse thoroughly with soap and water.  Use one suppository daily for seven days.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Borax 3X HPUS
Collinsonia Canadensis 3x HPUS
Berberis Vulgaris 6X HPUS
Hamamelis Virginiana 6X HPUS

Purpose

OTC - PURPOSE SECTION

Purpose

Temporary relief from symptoms of vaginal yeast infections

INDICATIONS & USAGE SECTION

Uses For the temporary relief of symptoms associated with vaginal yeast infection, including;

  • itching
  • burning
  • irritation

Warnings

WARNINGS SECTION

For vaginal use only. Use only as directed.

Do not use if you have never had a vaginal yeast infection diagnosed by a doctor.

OTC - STOP USE SECTION

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - ASK DOCTOR SECTION

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

OTC - WHEN USING SECTION

When using this product

  • if you do not get complete relief ask a doctor before using another product,

Directions

DOSAGE & ADMINISTRATION SECTION

Remove one suppository from the foil wrap and place in the applicator.  Insert suppository into the vagina with the applicator.  Remove applicator and cleanse thoroughly with soap and water.  Use one suppository daily for seven days.

Other information

OTHER SAFETY INFORMATION

Other Information

  • Suppositories are not a contraceptive and should not be used to prevent pregnancy.
  • Do not Use if foil seal on suppositories is torn, open or incompletely sealed, Purchase if carton is open
  • Store at room temperature
  • Lot number and expiration dates: see bottom of box

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Bacillus coagulans, Polyethylene Glycols

Questions or comments?

OTC - QUESTIONS SECTION

1-800-635-3696

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68093-7106-1Yeast Gard Advanced10 in 1 CARTONSUPPOSITORY102
68093-7106-1Yeast Gard Advanced1 in 1 PACKETSUPPOSITORY12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68093-7106YEAST GARD ADVANCED (BORAX, COLLINSONIA CANADENSIS, BERBERIS VULGARIS, HAMAMELIS VIRGINIANA) SUPPOSITORY [WISCONSIN PHARMACAL COMPANY]2Current NDC, Legacy NDC, 2 package rows20181212_b3f066d9-0f0f-455d-b1b1-dc13ba80fbfc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68093-710668093-7106-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYETHYLENE GLYCOL 400B697894SGQIACT
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
BACILLUS COAGULANSISK1LOY57EIACT
POLYETHYLENE GLYCOL 1450OJ4Z5Z32L4IACT
SODIUM BORATE91MBZ8H3QOACTIB
COLLINSONIA CANADENSIS ROOTO2630F3XDRACTIB
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKT7S323PKJSACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Yeast Gard AdvancedBORAX, COLLINSONIA CANADENSIS, BERBERIS VULGARIS, HAMAMELIS VIRGINIANAWisconsin Pharmacal Companyb3f066d9-0f0f-455d-b1b1-dc13ba80fbfc2018-12-06WarningsExact identifier
ndc (package): 68093-7106-1
ndc (product): 68093-7106
ndc11 (package): 68093710601
spl id: 7c5d8463-52ff-a397-e053-2991aa0abc29
spl set id: b3f066d9-0f0f-455d-b1b1-dc13ba80fbfc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.