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TERRAMED JUST THINK COMFORT GYNOCARE FOR BACTERIAL VAGINOSIS SYMPTOMS RELIEF sodium borate,calendula officinalis flowering top,goldenseal,olea europaea olive leaf powder 3 [hp_X]/2g; 1 [hp_X]/2g; 5 [hp_X]/2g; 3 [hp_X]/2g Suppository — NDC 83004-0041-01 package photo

TERRAMED JUST THINK COMFORT GYNOCARE FOR BACTERIAL VAGINOSIS SYMPTOMS RELIEF sodium borate,calendula officinalis flowering top,goldenseal,olea europaea olive leaf powder 3 [hp_X]/2g; 1 [hp_X]/2g; 5 [hp_X]/2g; 3 [hp_X]/2g Suppository

by Rida LLC · 12 BLISTER PACK in 1 CARTON (83004-041-01) / 2 g in 1 BLISTER PACK
NDC 83004-0041-01
🏷️ FDA NDC (as labeled) 83004-041-01 billing pads the product 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) 83004-041-01
Product NDC 83004-041
11-digit billing NDC 83004004101
UNII 91MBZ8H3QO, 18E7415PXQ, ZW3Z11D0JV, MJ95C3OH47
SPL Set ID 1625d88d-5ac8-492a-a152-3047d168575a
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-12-12
Route VAGINAL
Dosage form SUPPOSITORY
Substance SODIUM BORATE; CALENDULA OFFICINALIS FLOWERING TOP; GOLDENSEAL; OLEA EUROPAEA (OLIVE) LEAF POWDER
Why two NDCs? The FDA registers this code as 83004-041-01 — a 5-3-2 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 product segment → 83004-0041-01. 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

LabelerRida LLC
Labeler code83004
First marketedDec 2024
Product typeHuman Otc Drug
Portfolio47 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?

This is an unapproved homeopathic vaginal suppository containing calendula, goldenseal, olive leaf powder, and sodium borate. In homeopathic practice, these ingredients are traditionally used for symptoms associated with vaginal discomfort. Homeopathic products are marketed based on homeopathic tradition rather than clinical evidence, and the FDA does not evaluate them for safety or effectiveness. This product is not approved by the FDA.

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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII V1IA3S3CUS
    A plant extract derived from Cnidium monnieri fruit, commonly used in traditional Asian medicine preparations. In formulations, it may serve as an active botanical ingredient or flavoring agent, though its specific role depends on the product type.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII E849G4X5YJ
    Saffron is a natural spice derived from the crocus flower. It functions as a colorant and flavoring agent, giving medicines a yellow to orange hue and subtle taste.
  • UNII IYR6K8KQ5K
    A plant extract from sophora flavescens root used as a natural colorant and flavoring agent in medicines. It may also help preserve the product and provide texture.
  • UNII 1NT28V9397
    Thuja occidentalis is a plant extract from the evergreen arborvitae tree. It's used in some formulations as a flavoring agent or botanical ingredient.
  • UNII T7EV247N2B
    Tinospora cordifolia stem is a plant extract used as a natural filler and binding agent in medications. It helps hold tablet ingredients together and may add bulk to the formulation.

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

The official label also statesAloe Vera Extract, Cnidium Monnieri (Snake Seed) Extract, Coconut Oil, Crocus Sativus (Saffron) Extract, Sophora Flavescens Extract, Thuja Occidentalis (Yellow Cedar) Extract, Tinospora Cordifolia (Golden Vine) Extract, Tocopherol (Vitamin E).

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 eachPer 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
Terramed Just Think Comfort Gynocare For Bacterial Vaginosis Symptoms Relief 3 [hp_X]/2g; 1 [hp_X]/2g; 5 [hp_X]/2g; 3 [hp_X]/2gthis 83004-0041-01 Rida 2 g — — 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

🏛️
2024
On the market since
Dec 2024
📍
2026
Currently FDA-listed
2 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
83004-0041-01 You're viewing this 12 BLISTER PACK in 1 CARTON (83004-041-01) / 2 g in 1 BLISTER PACK 2024-12-12 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

TERRAMED JUST THINK COMFORT GYNOCARE FOR BACTERIAL VAGINOSIS SYMPTOMS RELIEF sodium borate,calendula officinalis flowering top,goldenseal,olea europaea olive leaf powder 3 [hp_X]/2g; 1 [hp_X]/2g; 5 [hp_X]/2g; 3 [hp_X]/2g SUPPOSITORY 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 83004-041-01, 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: 83004-0041-01, written without dashes as 83004004101. 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 83004-0041-01, the first segment (83004) is the labeler code FDA assigned to Rida LLC; the middle segment (0041) 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 Rida LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Rida LLC 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 13 words ▾

Uses For the temporary relief of minor vaginal discomfort and feelings of irritation.

⏱️ Dosage and Administration 36 words ▾

Directions Adults: insert one (1) suppository vaginally at bedtime. Use once daily for up to 7 consecutive nights. Do not use more than one suppository in any 24-hour period. Children under 12 years: ask a doctor.

⚠️ Warnings ~1 min read ▾

Warnings For vaginal use only . Do not swallow. For adult use only .

Do not use : if you have never had vaginal symptoms before if you are allergic to any of the ingredients in this product if you have fever, chills, abdominal pain, or pelvic pain if you have abnormal vaginal bleeding if the foil packet is damaged, torn, or previously opened. Ask a doctor before use if you have : diabetes, a weakened immune system, or a history of recurrent vaginal infections a serious medical condition or are under medical supervision; symptoms that have lasted more than 7 days before starting use. When using this product : you may experience mild burning, itching, or irritation at the application site. do not use tampons, douches, spermicides, or other vaginal products; this product may damage condoms and diaphragms and reduce their effectiveness. avoid contact with eyes.

Stop use and ask a doctor if : symptoms do not improve within 3 days symptoms last more than 7 days symptoms worsen or return after completion. new symptoms develop, including fever, rash, pelvic pain, nausea, or unusual bleeding severe burning, swelling, or rash occurs at the application site. If pregnant or breastfeeding , ask a healthcare professional before use. Keep out of reach of children .

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

🧪 Active Ingredient 20 words ▾

Active Ingredient Borax 3X HPUS (Sodium Borate), Calendula officinalis 1X HPUS, Hydrastis canadensis 5X HPUS, Olive Extract (Oleuropein) 3X HPUS.

🧪 Inactive Ingredients 32 words ▾

Inactive Ingredients Aloe Vera Extract, Cnidium Monnieri (Snake Seed) Extract, Coconut Oil, Crocus Sativus (Saffron) Extract, Sophora Flavescens Extract, Thuja Occidentalis (Yellow Cedar) Extract, Tinospora Cordifolia (Golden Vine) Extract, Tocopherol (Vitamin E).

🎯 Purpose 2 words ▾

Purpose Homeopathic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 83004-0040-01 · Rida 83004-0042-01 · Rida →
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.