Yeast Gard Homeopathic Gel

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 Homeopathic Gel Homeopathic Gel Treatment
Active ingredientHAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, COLLINSONIA CANADENSIS ROOT, SODIUM BORATE, BERBERIS VULGARIS ROOT BARK
Label structure9 sections

Dosage and administration

Directions Apply to affected area as often as needed. Because the area is irritated, you could experience a slight burning sensation. If this persists more than a few minutes, remove gel and discontinue use. Wash hand thoroughly with soap an dwater before and after use. Do not use for children under two years. Consult a doctor if condition persists.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Borax 3X HPUS

Collinsonia Canadensis 3X HPUS

Berberis Vulgaris 6X HPUS

Hamamelis Virginiana 6X HPUS

OTC - PURPOSE SECTION

Purpose Temporary relief from external vagianl discomfort including itching, burning, and irritation

INDICATIONS & USAGE SECTION

Uses For temporary relief of symptoms associate with vaginal yeast infection, including:itching, burning, and irritation.

Warnings

WARNINGS SECTION

For external vaginal use only. Use only as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medial help or contact a Poison Control Center right away. If in eyes, flush with water for 15 minutes and call a physician.

OTC - STOP USE SECTION

Stop use and ask doctor if

  • Symptoms worsen, last more than 7 days, or clear up and occur again within a few days.
  • You get a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge.

OTC - DO NOT USE SECTION

Do not use if

  • you have never had a vaginal yeast infection diagnosed by a doctor.

OTC - WHEN USING SECTION

When using this product

  • Wash hands thoroughly with soap and water before and after use
  • Avoid contact with eyes
  • If burning sensation occurs and lasts more than a few minutes, remove gel and discontinue use
  • Do not use more than one week unless directed by a doctor
  • If yoyu do not get complete relief ask a doctor before using another product.

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 - PREGNANCY OR BREAST FEEDING SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply to affected area as often as needed. Because the area is irritated, you could experience a slight burning sensation. If this persists more than a few minutes, remove gel and discontinue use.
  • Wash hand thoroughly with soap an dwater before and after use.
  • Do not use for children under two years. Consult a doctor if condition persists.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Allantoin, Benzalkonium Chloride 50%, Disodium EDTA, Glucono Delta Lactone, Polysorbate 20, Propanediol, Sodium Benzoate, Sodium Hydroxide, Tea Tree Oil, Water, Xanthan Gum

Other Information

OTHER SAFETY INFORMATION

Other information

  • Do not use if safety seal under cap is missing or broken
  • Store at room temperature
  • Lot number and expiration date: see date on tube and box flap.
  • Retain carton for complete Drug Facts Warnings
  • There is no scientific evidence that this product works. Ther product claims are based on theories of homeopathy from the 1700's that are not accepted by most modern medical experts.

OTC - QUESTIONS SECTION

Questions or comments? 1-800-635-3696

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tubetubecartoncarton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68093-7247-1Yeast Gard Homeopathic GelHomeopathic Gel Treatment1 in 1 CARTONGEL12
68093-7247-1Yeast Gard Homeopathic GelHomeopathic Gel Treatment28.35 g in 1 TUBEGEL28.352

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68093-7247YEAST GARD HOMEOPATHIC GEL HOMEOPATHIC GEL TREATMENT (BORAX, COLLINSONIA CANADENSIS, BERBERIS VULGARIS, HAMAMELIS VIRGINIANA) GEL [WISCONSIN PHARMACAL COMPANY]2Current NDC, Legacy NDC, 2 package rows20181212_de4dc2a2-b829-4b1b-8813-94700315a7bc.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68093-724768093-7247-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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 Homeopathic Gel Homeopathic Gel TreatmentBORAX, COLLINSONIA CANADENSIS, BERBERIS VULGARIS, HAMAMELIS VIRGINIANAWisconsin Pharmacal Companyde4dc2a2-b829-4b1b-8813-94700315a7bc2018-12-06WarningsExact identifier
ndc (package): 68093-7247-1
ndc (product): 68093-7247
ndc11 (package): 68093724701
spl id: 7c5d8463-52e0-a397-e053-2991aa0abc29
spl set id: de4dc2a2-b829-4b1b-8813-94700315a7bc

Reported adverse events (FAERS/openFDA)#

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