Home › NDC Lookup › Ingredients › Apis Mellifica, Calendula Officinalis, E... › 83570-0009-01
OWELL NATURALS DRAW MAX Apis mellifica, Calendula officinalis, Echinacea purpurea, Hepar sulphuris calcareum, Ledum palustre, Urtica dioica 10 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 10 [hp_X]/g; 6 [hp_X]/g; 3 [hp_X]/g Ointment, 28.3 g — NDC 83570-0009-01 package photo

OWELL NATURALS DRAW MAX Apis mellifica, Calendula officinalis, Echinacea purpurea, Hepar sulphuris calcareum, Ledum palustre, Urtica dioica 10 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 10 [hp_X]/g; 6 [hp_X]/g; 3 [hp_X]/g Ointment, 28.3 g

by OWELL NATURALS LLC · 28.3 g in 1 JAR (83570-009-01)
NDC 83570-0009-01
🏷️ FDA NDC (as labeled) 83570-009-01 billing pads the product segment with a zero
This package
Contains28.3 g Pack sizes2 compare ↓
Also comes in: 56.7 g 83570-0009-02
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) 83570-009-01
Product NDC 83570-009
11-digit billing NDC 83570000901
UNII 7S82P3R43Z, 18E7415PXQ, QI7G114Y98, 1MBW07J51Q, 877L01IZ0P, 710FLW4U46
UPC 0850057105551, 0850057105568
SPL Set ID 57b30ce7-31c3-ed55-e063-6294a90a68f3
Established class (EPC) Standardized Insect Venom Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Bee Venoms
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-28
Route TOPICAL
Dosage form OINTMENT
Substance APIS MELLIFERA; CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA PURPUREA; CALCIUM SULFIDE; LEDUM PALUSTRE TWIG; URTICA DIOICA
Why two NDCs? The FDA registers this code as 83570-009-01 — 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 → 83570-0009-01. 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

LabelerOWELL NATURALS LLC
Labeler code83570
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio2 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?

Owell Naturals Draw Max is a topical ointment containing six ingredients prepared according to homeopathic principles. The product includes honey bee extract, calendula flower, echinacea, calcium sulfide, ledum, and nettle. In homeopathic practice, these ingredients are traditionally used to address minor skin concerns. This is an unapproved homeopathic product marketed based on homeopathic tradition rather than FDA evaluation 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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • UNII 75IZZ8Y727
    Camphor oil is a colorless to pale yellow essential oil derived from the camphor laurel tree. It's used in medicines as a flavoring agent and mild skin-soothing ingredient in topical formulations.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • 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 ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII LAV5U5022Y
    Methyl salicylate is a naturally derived liquid compound commonly found in wintergreen plants. In medicines, it's used as a flavoring agent and penetrating solvent to help distribute active ingredients evenly throughout topical products.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • UNII 5EXL5H740Y
    A natural oil extracted from Scotch pine needles, used as a flavoring agent and fragrance component in medicines. It adds taste and aroma to improve how the medication tastes or smells.

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

The official label also statesBeeswax, Camphor oil, Castor oil, Eucalyptus oil, Lavender oil, Olive oil, Pine needle oil, Methyl salicylate.

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.
Try another pack size: 56.7 g
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
Owell Naturals Draw Max 10 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 10 [hp_X]/g; 6 [hp_X]/g; 3 [hp_X]/gthis 83570-0009-01 OWELL 28.3 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

🏛️
2026
On the market since
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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
83570-0009-01 You're viewing this 28.3 g in 1 JAR (83570-009-01) 2026-07-28 Active
83570-0009-02 56.7 g in 1 JAR (83570-009-02) 2026-07-28 Active

Pack size FAQ

What quantity is in NDC 83570-0009-01?
NDC 83570-0009-01 contains 28.3 g — 28.3 g in 1 jar.
What is the difference between NDC 83570-0009-01 and NDC 83570-0009-02?
Both are OWELL NATURALS DRAW MAX Apis mellifica, Calendula officinalis, Echinacea purpurea, Hepar sulphuris calcareum, Ledum palustre, Urtica dioica 10 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 10 [hp_X]/g; 6 [hp_X]/g; 3 [hp_X]/g Ointment — the drug itself is identical. NDC 83570-0009-01 is the 28.3 g package, while NDC 83570-0009-02 is the 56.7 g package.
What NDC number is used to bill for this package of OWELL NATURALS DRAW MAX Apis mellifica, Calendula officinalis, Echinacea purpurea, Hepar sulphuris calcareum, Ledum palustre, Urtica dioica 10 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 10 [hp_X]/g; 6 [hp_X]/g; 3 [hp_X]/g Ointment?
Bill NDC 83570-0009-01 — the 11-digit billing format is 83570000901. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

OWELL NATURALS DRAW MAX Apis mellifica, Calendula officinalis, Echinacea purpurea, Hepar sulphuris calcareum, Ledum palustre, Urtica dioica 10 [hp_X]/g; 1 [hp_X]/g; 3 [hp_X]/g; 10 [hp_X]/g; 6 [hp_X]/g; 3 [hp_X]/g 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 83570-009-01, 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: 83570-0009-01, written without dashes as 83570000901. 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 83570-0009-01, the first segment (83570) is the labeler code FDA assigned to OWELL NATURALS LLC; the middle segment (0009) 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 OWELL NATURALS 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 56.7 g (83570-0009-02). 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?
OWELL NATURALS 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 17 words ▾

Uses For temporary relief of minor skin irritations, insect bites, stings, rashes, minor cuts, scrapes, and splinters.

⏱️ Dosage and Administration 35 words ▾

Directions Adults and children 2 years of age and older: Apply a thin layer to the affected area 2 to 3 times daily or as needed. Children under 2 years of age: Consult a physician.

⚠️ Warnings 29 words ▾

Warning For external use only. Do not use on: Deep or puncture wounds Animal bites Serious burns When using this product: Do not get into eyes or mucous membranes.

📦 Storage and Handling 18 words ▾

Storage Store at room temperature 20°–25°C (68°–77°F). Keep tightly closed and protect from excessive heat or direct sunlight.

🧪 Active Ingredient 27 words ▾

Active ingredients Apis mellifera 10X HPUS Calendula officinalis 1X HPUS Echinacea purpurea 3X HPUS Hepar sulphuris calcareum 10X HPUS Ledum palustre 6X HPUS Urtica dioica 3X HPUS

🧪 Inactive Ingredients 18 words ▾

Inactive Ingredients Beeswax, Camphor oil, Castor oil, Eucalyptus oil, Lavender oil, Olive oil, Pine needle oil, Methyl salicylate.

🎯 Purpose 14 words ▾

Purpose Anti-itch / Pain Relief Healing Agent Natural Antiseptic Skin Relief Anti-inflammatory Rash Relief

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 83570-0008-01 · OWELL 83570-0443-02 · OWELL →
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.