Terramed Just Think Comfort Hemorrhoid Fissure Treatment Aesculus hippocastanum,Hamamelis virginiana,Paeonia officinalis 7 [hp_X]/35g; 2 [hp_X]/35g; 2 [hp_X]/35g; 7 [hp_X]/35g Ointment — NDC 83004-0021-01 package photo

Terramed Just Think Comfort Hemorrhoid Fissure Treatment Aesculus hippocastanum,Hamamelis virginiana,Paeonia officinalis 7 [hp_X]/35g; 2 [hp_X]/35g; 2 [hp_X]/35g; 7 [hp_X]/35g Ointment

by Rida LLC · 7 APPLICATOR in 1 BOX (83004-021-01) / 35 g in 1 APPLICATOR
NDC 83004-0021-01
🏷️ FDA NDC (as labeled) 83004-021-01 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 →

🆔 Identity & classification

FDA NDC (as labeled) 83004-021-01
Product NDC 83004-021
11-digit billing NDC 83004002101
UNII 3C18L6RJAZ, 8FP93ED6H2, S3Q2X90SUF, P29ZH1A35Z
SPL Set ID fb40241b-2239-4b82-806b-da152e1332c4
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-03-13
Route TOPICAL
Dosage form OINTMENT
Substance HORSE CHESTNUT; HAMAMELIS VIRGINIANA LEAF WATER; PAEONIA OFFICINALIS WHOLE; KRAMERIA LAPPACEA ROOT
Why two NDCs? The FDA registers this code as 83004-021-01 — 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 → 83004-0021-01. 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 marketedMar 2025
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?

Terramed Just Think Comfort is a topical ointment containing herbal ingredients used in homeopathic practice. The product includes witch hazel, horse chestnut, krameria root, and peony, which are traditionally used in homeopathic preparations for conditions affecting the rectal area. As a homeopathic product, it is marketed based on homeopathic tradition and theory rather than clinical evidence evaluated by the FDA for safety or effectiveness.

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 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII ZF94AP8MEY
    Hydrogenated castor oil is a processed plant oil made by adding hydrogen to castor oil. It's used as a binder to help hold tablet ingredients together and as a lubricant to prevent sticking during manufacturing.
  • UNII 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII F4VNO44C09
    Linalool is a natural fragrant compound found in flowers and plants. It's added to medicines as a flavor and scent agent to improve taste and aroma.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • 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.

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

The official label also statesLanolin, Glyceryl Stearate, Petrolatum, Cetearyl Alcohol, Hydrogenated Castor Oil, Glycerin, Menthol, Eucalyptus Globulus (Eucalyptus) Oil, Tea Tree Oil, Linalool

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 DailyMedingredient 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
Terramed Just Think Comfort Hemorrhoid Fissure Treatment 7 [hp_X]/35g; 2 [hp_X]/35g; 2 [hp_X]/35g; 7 [hp_X]/35gthis 83004-0021-01 Rida 7 applicators 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

🏛️
2025
On the market since
Mar 2025
📍
2026
Currently FDA-listed
1 year 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
83004-0021-01 You're viewing this 7 APPLICATOR in 1 BOX (83004-021-01) / 35 g in 1 APPLICATOR 2025-03-13 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Terramed Just Think Comfort Hemorrhoid Fissure Treatment Aesculus hippocastanum,Hamamelis virginiana,Paeonia officinalis 7 [hp_X]/35g; 2 [hp_X]/35g; 2 [hp_X]/35g; 7 [hp_X]/35g OINTMENT 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 83004-021-01, 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: 83004-0021-01, written without dashes as 83004002101. 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 83004-0021-01, the first segment (83004) is the labeler code FDA assigned to Rida LLC; the middle segment (0021) 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 24 words

Uses Temporarily Relives symptoms of hemorrhoids such as: • Burning • Itching • Swelling • Pain • Discomfort • Relives hemorrhoids symptoms following childbirth

⏱️ Dosage and Administration 150 words

Directions Step 1 - Cleanse: Thoroughly wash the affected area with mild soap and warm water. Pat dry gently with a clean, soft cloth. Step 2 - Preparation: Open the Recral pre-filled applicator packaging and remove the applicator.

Hold it upright with the cap on. Step 3- Unscrew Cap: Unscrew the cap gently from the pre-filled applicator. Make sure not to squeeze the tube during this process.

Step 4- Positioning: Gently and carefully insert the rounded tip of the applicator into the rectum, following the natural curvature. Step 5- Application: Squeeze the applicator gently to dispense the recommended dose of the treatment. Slowly withdraw the applicator while continuing to apply the treatment.

Step 6 - Dispose: After use, discard the applicator and cap in a suitable waste bin. Do not flush the applicator down the toilet. Step 7 - Hygiene: Cleanse your hands thoroughly with soap and water after use.

⚠️ Warnings 47 words

Warnings For rectal use only. Ask a doctor before use in case of bleeding. When using this product , do not exceed the recommended daily dosage unless directed by a doctor. Stop use and ask a doctor if symtoms persist for more than 7 days or worsen.

🧪 Active Ingredient 63 words

Active Ingredient Aesculus hippocastanum 7X HPUS (0.01 g)........................Reduces swelling and relieves stinging pain associated with external hemorrhoids Hamamelis virginiana 2X HPUS (0.01 g)............................................Relieves burning, itching, and discomfort associated with hemorrhoids Paeonia officinalis (Peony) 2X H PUS (0.01 g)........................................Relieves burning pain and cozing associated with external hemorrhoids Ratanhia 7X HPUS (0.01 g)................................................................Relieves itching and discomfort from external hemorrhoids, especially during and after bowel movements

🧪 Inactive Ingredients 21 words

Inactive ingredients Lanolin, Glyceryl Stearate, Petrolatum, Cetearyl Alcohol, Hydrogenated Castor Oil, Glycerin, Menthol, Eucalyptus Globulus (Eucalyptus) Oil, Tea Tree Oil, Linalool

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