Home › NDC Lookup › Ingredients › Pulsatilla Pratensis Whole,Sodium Borate... › 83004-0043-01
💊image loading
(from DailyMed)

Terramed Just Think Comfort Homeopathic Vaginal Treatment for Yeast Infection Symptoms Relief pulsatilla pratensis whole,sodium borate,calendula officinalis flowering top,olea europaea olive leaf 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4g Suppository — NDC 83004-043-01 (Billing 83004-0043-01)

by Rida LLC · 12 PACKET in 1 BOX / 4 g in 1 PACKET

This is a package of Terramed Just Think Comfort Homeopathic Vaginal Treatment for Yeast Infection Symptoms Relief pulsatilla pratensis whole,sodium borate,calendula officinalis flowering top,olea europaea olive leaf 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4g Suppository from Rida LLC, marketed since Dec 2024 and currently FDA-listed. It is this product's only package size.

NDC 83004-0043-01
🏷️ FDA NDC (as labeled) 83004-043-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

NDC database record

One package, one record: these facts belong to NDC 83004-043-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
83004 labeler · 043 product · 01 package
Package marketed since
Dec 12, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8300404301 4
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83004-043-01
Product NDC 83004-043
11-digit billing NDC 83004004301
UNII 8E272251DI, 91MBZ8H3QO, 18E7415PXQ, MJ95C3OH47
SPL Set ID 08d6e79d-67a7-49af-a095-68ac40218311
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 PULSATILLA PRATENSIS WHOLE; SODIUM BORATE; CALENDULA OFFICINALIS FLOWERING TOP; OLEA EUROPAEA (OLIVE) LEAF POWDER
Why two NDCs? The FDA registers this code as 83004-043-01 — 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 → 83004-0043-01. 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.

Clinical

🧪 What is this product?

This is a homeopathic vaginal suppository containing calendula, olive leaf, pulsatilla, and sodium borate. Homeopathic products are marketed based on traditional homeopathic practice and have not been evaluated by the FDA for effectiveness. In homeopathic tradition, these ingredients are typically used to address symptoms associated with yeast infections, though homeopathic remedies work according to homeopathic principles rather than conventional medical mechanisms. This product is not proven to be effective by FDA standards.

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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
83004-0043-01 You're viewing this Main listing 12 PACKET in 1 BOX / 4 g in 1 PACKET 2024-12-12 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Terramed Just Think Comfort Homeopathic Vaginal Treatment for Yeast Infection Symptoms Relief 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4gthis 83004-0043-01 Rida 12 packets — — 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.

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 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 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 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 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 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.

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

The official label also statesAloe Vera Leaf Extract, Coconut (Cocos Nucifera) Oil, Saffron (Crocus Sativus) Extract, Yellow Cedar (Thuja Occidentalis) Extract, Tocopherol (Vitamin E), Purified Water.

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.

Manufacturer & labeler

LabelerRida LLC
Labeler code83004
First marketedDec 2024
Product typeHuman Otc Drug
Portfolio47 products on file

More NDCs from Rida LLC labeler code 83004

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.

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 19 words ▾

Uses For the temporary relief of symptoms associated with: minor intimate irritation; minor burning, itching, and discomfort; intimate odor.

⏱️ 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 18 years: do not use.

⚠️ Warnings ~1 min read ▾

Warnings For vaginal use only. For adult use only. Do not use : if you are pregnant or breastfeeding, unless directed by a doctor if you have pelvic pain, fever, chills, or abnormal vaginal bleeding if you have unusual discharge with a foul odor if you have never had vaginal symptoms before if you are allergic to any ingredient in this product if the foil packet is damaged, torn, or previously opened Ask a doctor before use if you have : diabetes, a weakened immune system, or 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 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, 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 17 words ▾

Active Ingredient Pulsatilla pratensis 5X HPUS, Borax 5X HPUS, Calendula officinalis 5X HPUS, Olea europaea 5X HPUS.

🧪 Inactive Ingredients 24 words ▾

Inactive Ingredients Aloe Vera Leaf Extract, Coconut (Cocos Nucifera) Oil, Saffron (Crocus Sativus) Extract, Yellow Cedar (Thuja Occidentalis) Extract, Tocopherol (Vitamin E), Purified Water.

🎯 Purpose 17 words ▾

Purpose For symptoms of intimate irritation; for symptoms of burning and discomfort; for symptoms of intimate discomfort.

📄 Package Label / Principal Display Panel 4 words ▾

Product label image description

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Terramed Just Think Comfort Homeopathic Vaginal Treatment for Yeast Infection Symptoms Relief pulsatilla pratensis whole,sodium borate,calendula officinalis flowering top,olea europaea olive leaf 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4g; 5 [hp_X]/4g 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 — Not published for this NDC No photo available yet for this listing.
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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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.
← 83004-0042-01 · Rida 83004-0044-01 · 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.