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Yeast Gard Homeopathic Gel Homeopathic Gel Treatment Borax, Collinsonia Canadensis, berberis Vulgaris, Hamamelis Virginiana 6 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 6 [hp_X]/g Gel, 1 tube — NDC 68093-7247-01 package photo

Yeast Gard Homeopathic Gel Homeopathic Gel Treatment Borax, Collinsonia Canadensis, berberis Vulgaris, Hamamelis Virginiana 6 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 6 [hp_X]/g Gel, 1 tube

by Wisconsin Pharmacal Company · 1 TUBE in 1 CARTON (68093-7247-1) / 28.35 g in 1 TUBE
NDC 68093-7247-01
🏷️ FDA NDC (as labeled) 68093-7247-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 68093-7247-1
Product NDC 68093-7247
11-digit billing NDC 68093724701
UNII T7S323PKJS, O2630F3XDR, 91MBZ8H3QO, 1TH8Q20J0U
UPC 0012277665011
SPL Set ID de4dc2a2-b829-4b1b-8813-94700315a7bc
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2007-04-01
Route VAGINAL
Dosage form GEL
Substance HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; COLLINSONIA CANADENSIS ROOT; SODIUM BORATE; BERBERIS VULGARIS ROOT BARK
Why two NDCs? The FDA registers this code as 68093-7247-1 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 68093-7247-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerWisconsin Pharmacal Company
Labeler code68093
First marketedApr 2007
Product typeHuman Otc Drug
Portfolio16 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

Yeast Gard is a homeopathic vaginal gel containing herbal and mineral ingredients including berberis vulgaris, collinsonia canadensis, hamamelis virginiana, and sodium borate. In homeopathic practice, these ingredients are traditionally used to address vaginal discomfort and irritation. This is an unapproved homeopathic product marketed based on homeopathic tradition; homeopathic products are not evaluated by the FDA for effectiveness.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII XDK458E1J9
    Allantoin is a naturally occurring compound that softens and soothes skin. In medicines, it acts as a skin-conditioning agent and helps promote healing and moisturizing in topical products.
  • UNII F5UM2KM3W7
    Benzalkonium chloride is a chemical compound that works as a preservative and antimicrobial agent in medications. It prevents bacterial and fungal growth in liquid formulations to keep the product safe during storage and use.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII WQ29KQ9POT
    Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

11 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAllantoin, Benzalkonium Chloride 50%, Disodium EDTA, Glucono Delta Lactone, Polysorbate 20, Propanediol, Sodium Benzoate, Sodium Hydroxide, Tea Tree Oil, Water, Xanthan Gum

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Yeast Gard Homeopathic Gel Homeopathic Gel Treatment 6 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 6 [hp_X]/gthis 68093-7247-01 Wisconsin 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2007
On the market since
Apr 2007
📍
2026
Currently FDA-listed
19 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Borax, Collinsonia Canadensis, berberis Vulgaris, Hamamelis Virginiana — the ingredient across all brands.

Top reported reactions

Drug Interaction1
Homicidal Ideation1

Reporter sex

1 reports
Female · 100%
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
68093-7247-01 You're viewing this 1 TUBE in 1 CARTON (68093-7247-1) / 28.35 g in 1 TUBE 2007-04-01 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Yeast Gard Homeopathic Gel Homeopathic Gel Treatment Borax, Collinsonia Canadensis, berberis Vulgaris, Hamamelis Virginiana 6 [hp_X]/g; 3 [hp_X]/g; 3 [hp_X]/g; 6 [hp_X]/g GEL is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 68093-7247-1, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 68093-7247-01, written without dashes as 68093724701. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 68093-7247-01, the first segment (68093) is the labeler code FDA assigned to Wisconsin Pharmacal Company; the middle segment (7247) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Wisconsin Pharmacal Company. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Wisconsin Pharmacal Company is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 15 words ▾

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

⏱️ Dosage and Administration 60 words ▾

Directions 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.

⚠️ Warnings ~1 min read ▾

Warnings For external vaginal use only. Use only as directed. 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. 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. Do not use if you have never had a vaginal yeast infection diagnosed by a doctor. 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.

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

🧪 Active Ingredient 17 words ▾

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

🧪 Inactive Ingredients 24 words ▾

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

🎯 Purpose 12 words ▾

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

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 68093-7245-01 · Wisconsin 68093-7426-01 · Wisconsin →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.