Home › NDC Lookup › Ingredients › Olibanum, Thuja Occidentalis, Gelsemium... › 59623-0006-02
Cedar X Formula Olibanum, Thuja Occidentalis, Gelsemium Sempervirens, Allium Cepa, Antimonium Tartaricum, Hepar Sulphuris Calcareum, Juniperus Communis. 3 [hp_X]/mL; 3 [hp_X]/mL; 4 [hp_X]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 30 [hp_C]/mL Liquid, 59 mL — NDC 59623-0006-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Cedar X Formula Olibanum, Thuja Occidentalis, Gelsemium Sempervirens, Allium Cepa, Antimonium Tartaricum, Hepar Sulphuris Calcareum, Juniperus Communis. 3 [hp_X]/mL; 3 [hp_X]/mL; 4 [hp_X]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 30 [hp_C]/mL Liquid, 59 mL — NDC 59623-006-02 (Billing 59623-0006-02)

by Integrative Healing Institute, LLC · 59 mL in 1 BOTTLE, DROPPER

This is a package of 59 mL of Cedar X Formula Olibanum, Thuja Occidentalis, Gelsemium Sempervirens, Allium Cepa, Antimonium Tartaricum, Hepar Sulphuris Calcareum, Juniperus Communis. 3 [hp_X]/mL; 3 [hp_X]/mL; 4 [hp_X]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 30 [hp_C]/mL Liquid from Integrative Healing Institute, LLC, marketed since Nov 2013 and currently FDA-listed.

NDC 59623-0006-02
🏷️ FDA NDC (as labeled) 59623-006-02 billing pads the product segment with a zero
This package
Contains59 mL Pack sizes2 compare ↓
Product page 59623-0006-01 Also comes in: 30 ml 59623-006-01
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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 59623-006-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
59623 labeler · 006 product · 02 package
Package marketed since
Nov 5, 2013
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0000309508627
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 59623-006-02
Product NDC 59623-006
11-digit billing NDC 59623000602
UNII R9XLF1R1WM, 1NT28V9397, 639KR60Q1Q, 492225Q21H, DL6OZ476V3, 1MBW07J51Q +1 more
UPC 0000309508627
SPL Set ID 8ab87e13-99ad-4b25-a0c3-e46a868cc684
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens; Dietary Proteins; Vegetable Proteins; Plant Proteins; Food Additives
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-11-05
Route ORAL
Dosage form LIQUID
Substance FRANKINCENSE; THUJA OCCIDENTALIS LEAFY TWIG; GELSEMIUM SEMPERVIRENS ROOT; ONION; ANTIMONY POTASSIUM TARTRATE; CALCIUM SULFIDE; JUNIPER BERRY
Why two NDCs? The FDA registers this code as 59623-006-02 — 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 → 59623-0006-02. 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?

Cedar X Formula is an oral liquid homeopathic product containing multiple plant and mineral ingredients including frankincense, thuja, gelsemium, onion, juniper berry, and antimony potassium tartrate. In homeopathic practice, these ingredients are traditionally prepared at various dilutions and are used by practitioners for respiratory and general wellness support. Homeopathic products are marketed based on traditional homeopathic theories and have not been evaluated by the FDA for safety or 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.

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 mLPer 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.
Try another pack size: 30 ml
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
59623-0006-01 59623-006-01 Main listing 30 mL in 1 BOTTLE, DROPPER 2013-11-05 — Active
59623-0006-02 You're viewing this 59 mL in 1 BOTTLE, DROPPER 2013-11-05 — Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 59 mL — 59 ml in 1 bottle, dropper.
How does this package differ from NDC 59623-0006-01?
Both are Cedar X Formula Olibanum, Thuja Occidentalis, Gelsemium Sempervirens, Allium Cepa, Antimonium Tartaricum, Hepar Sulphuris Calcareum, Juniperus Communis. 3 [hp_X]/mL; 3 [hp_X]/mL; 4 [hp_X]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 30 [hp_C]/mL Liquid — the drug itself is identical. This page's package is the 59 mL one, while NDC 59623-0006-01 is the 30 ml package.
What NDC number is used to bill for this package of Cedar X Formula Olibanum, Thuja Occidentalis, Gelsemium Sempervirens, Allium Cepa, Antimonium Tartaricum, Hepar Sulphuris Calcareum, Juniperus Communis. 3 [hp_X]/mL; 3 [hp_X]/mL; 4 [hp_X]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 30 [hp_C]/mL Liquid?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cedar X Formula 3 [hp_X]/mL; 3 [hp_X]/mL; 4 [hp_X]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 30 [hp_C]/mLthis 59623-0006-02 Integrative 59 ml — — 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

🏛️
2013
On the market since
Nov 2013
📍
2026
Currently FDA-listed
13 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 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • 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.

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

The official label also statesInactive ingredients: Citric Acid, Potassium Sorbate, 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

LabelerIntegrative Healing Institute, LLC
Labeler code59623
First marketedNov 2013
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from Integrative Healing Institute, LLC labeler code 59623

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 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 20 words ▾

Use: This product is a Homeopathic Dilution, formulated to support the body's immunity for the temporary relief of cedar allergies.

⏱️ Dosage and Administration 54 words ▾

Directions: Shake bottle well before use. Adults (12 and Older) Take 10 drops orally 1-3 times a day as needed. Children (11 and Younger) Take 6 drops orally 1-3 times a day as needed or as directed by your health care provider. Consult a Physician for use in children under 12 years of age.

⚠️ Warnings 39 words ▾

Warnings : Use only as directed. Stop use and consult a doctor if symptoms worsen or do not improve after 5 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children.

🧪 Active Ingredient 23 words ▾

Active ingredients: Olibanum 3X, Thuja Occidentalis 3X, Gelsemium Sempervirens 4X, Allium Cepa 6C, Antimonium Tartaricum 6C, Hepar Sulphuris Calcareum 6C, Juniperus Communis 30C.

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients: Citric Acid, Potassium Sorbate, Purified Water.

🎯 Purpose 15 words ▾

Purpose: Relief from sinus congestion, sneezing, runny nose, red itchy eyes, fatigue, wheezing and coughing.

📄 Keep Out of Reach of Children 7 words ▾

Keep out of the reach of children.

📄 Other Information 31 words ▾

Other information: Do not use if TAMPER EVIDENT seal around neck is broken or missing. Store at room temperature.

Mfg. by: OHM Pharma, Inc., Mineral Wells, TX 76067 Made in USA

📄 Questions or Comments 9 words ▾

INTEGRATIVE HEALING INSTITUTE San Antonio, TX 78216 integrativehealingsa.com 1.888.841.4034

📄 Package Label / Principal Display Panel 35 words ▾

INTEGRATIVE HEALING INSTITUTE HOMEOPATHIC MEDICINE NDC: 59623-006-01 NDC: 59623-006-02 CEDAR X FORMULA SAFE NATURAL EFFECTIVE ALCOHOL FREE NET 1 fl oz (30 mL) NET 2 fl oz (60 mL) 1oz bottle label 2oz bottle label

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

Cedar X Formula Olibanum, Thuja Occidentalis, Gelsemium Sempervirens, Allium Cepa, Antimonium Tartaricum, Hepar Sulphuris Calcareum, Juniperus Communis. 3 [hp_X]/mL; 3 [hp_X]/mL; 4 [hp_X]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 6 [hp_C]/mL; 30 [hp_C]/mL LIQUID 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 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 Integrative Healing Institute, LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 30 ml (59623-0006-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Integrative Healing Institute, 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.
← 59623-0001-01 · Integrative 59623-0013-01 · Integrative →
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.