Home › NDC Lookup › Ingredients › Sulfur, Graphite, Daphne Mezereum Bark,... › 43689-0035-01
Magnilife Eczema Care SULFUR, GRAPHITE, DAPHNE MEZEREUM BARK, TOXICODENDRON PUBESCENS WHOLE 1 [hp_X]/g; 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/g Cream — NDC 43689-0035-01 package photo

Magnilife Eczema Care SULFUR, GRAPHITE, DAPHNE MEZEREUM BARK, TOXICODENDRON PUBESCENS WHOLE 1 [hp_X]/g; 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/g Cream

by The Magni Group, Inc. · 1 JAR in 1 BOX, UNIT-DOSE (43689-0035-1) / 56 g in 1 JAR
NDC 43689-0035-01
🏷️ FDA NDC (as labeled) 43689-0035-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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) 43689-0035-1
Product NDC 43689-0035
11-digit billing NDC 43689003501
UNII 70FD1KFU70, 4QQN74LH4O, X2N6E405GV, C1S185Y74S
UPC 0723122170511
Application # M006
SPL Set ID 8e3fc743-4c82-4a03-a963-2d5f93a1bc26
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-09
Route TOPICAL
Dosage form CREAM
Substance SULFUR; GRAPHITE; DAPHNE MEZEREUM BARK; TOXICODENDRON PUBESCENS WHOLE
Why two NDCs? The FDA registers this code as 43689-0035-1 — a 5-4-1 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 package segment → 43689-0035-01. 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

LabelerThe Magni Group, Inc.
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code43689
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio4 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?

Magnilife Eczema Care is a topical cream marketed as an over-the-counter monograph product. It contains four herbal and mineral ingredients: sulfur, graphite, daphne mezereum bark, and toxicodendron pubescens whole. Sulfur is commonly used in skin preparations for its traditional role in addressing various skin conditions. The other three ingredients are plant and mineral substances that appear in topical products intended to support skin health.

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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 2FXJ6SW4PK
    A plant extract from yarrow, used in some formulations as a natural flavoring agent or botanical ingredient to add taste or aroma to the medicine.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • UNII E4F12ROE70
    A refined mineral oil derived from crude petroleum containing 13 to 14 carbon chains. It acts as a solvent, emollient, and carrier in topical formulations to help dissolve active ingredients and improve product texture and spreadability.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII H02N5LQ5F6
    A fragrant extract from sweet orange blossoms. It's used as a flavor and scent ingredient to make the medicine smell and taste better.
  • UNII VB06AV5US8
    Echinacea angustifolia is a plant extract used as a natural flavoring or coloring agent in some medicines. It may also help preserve the product's stability or serve as a filler ingredient.
  • UNII MJ2YTT4J8M
    Ethyl linoleate is a fatty acid ester derived from linoleic acid. It acts as an emollient and solvent in formulations, helping to dissolve or carry active ingredients and improve product texture and absorption.
  • UNII G3QC02NIE6
    Fennel seed is a plant-derived ingredient used as a flavoring agent in medicines. It adds taste to make the product more palatable, especially in liquid or chewable formulations.
  • UNII 93IXI5B6OJ
    A plant-derived ingredient from geranium root, traditionally used in herbal formulations. It may serve as a natural binder or contribute to the product's herbal content and stability.
  • 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 NT00Y05A2V
    A liquid extract from witch hazel plant leaves and twigs. It's used in topical products as an astringent agent and to help deliver other active ingredients into the skin.
  • UNII Z95S6G8201
    A synthetic surfactant derived from lauryl alcohol and ethylene oxide. It helps dissolve and mix oily and watery ingredients in liquid formulations, and may improve how the medicine spreads or is absorbed.
  • 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 B3AWW0N3GM
    Oleyl lactate is a synthetic ester made from oleic acid and lactic acid. It serves as an emollient and skin-conditioning agent in topical medicines, helping to soften and smooth the formulation while improving how it spreads on the skin.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • 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 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 81MCR2UQ6Q
    Rosa canina flower is a plant-derived ingredient from the wild rose plant. It's used in medicines as a natural flavoring agent and may also provide color or antioxidant properties to the formulation.
  • UNII 065C5D077J
    Sage is a natural plant extract used in medicines as a flavoring agent and preservative. It may help mask bitter tastes and extend shelf life in certain formulations.
  • UNII 07V4DX094T
    Sambucus nigra flower is an extract from the black elderflower plant. It may be added to medicines as a flavoring or coloring agent, or to provide traditional herbal characteristics to the formulation.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII X045WJ989B
    Sorbic acid is a preservative derived from berries that prevents mold, yeast, and bacterial growth in medicines. It keeps the product stable and safe during storage.
  • 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.
  • 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.

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

The official label also statesAchillea Millefolium Extract, Alcohol, Aloe Barbadensis Leaf Extract, Benzoic Acid, Beta-Glucan, C13-14 Isoparaffin, Calendula Officinalis Flower Extract, Carbomer, Chamomilla Recutita (Matricaria) Flower Extract, Citrus Aurantium Dulcis (Orange) Flower Extract, Echinacea Angustifolia Extract, Ethyl Linoleate, Foeniculum Vulgare (Fennel) Seed Extract, Geranium Maculatum Extract, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, lnulin, Laureth-7, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methyl Salicylate, Oleyl Lactate, Phenoxyethanol, Polyacrylamide, Potassium Sorbate, Propylene Glycol, Rosa Canina Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Sambucus Nigra Flower Extract, Sodium Benzoate, Sodium Hydroxide, Sorbic Acid, Tocopheryl Acetate, Water (Aqua), Yogurt Powder

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.
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
Magnilife Eczema Care 1 [hp_X]/g; 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/gthis 43689-0035-01 The 1 jar — — 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
43689-0035-01 You're viewing this 1 JAR in 1 BOX, UNIT-DOSE (43689-0035-1) / 56 g in 1 JAR 2026-07-09 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
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 "Otc Monograph Drug". 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 43689-0035-1, 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: 43689-0035-01, written without dashes as 43689003501. 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 43689-0035-01, the first segment (43689) is the labeler code FDA assigned to The Magni Group, Inc.; the middle segment (0035) 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 The Magni Group, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
The Magni Group, Inc. 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 11 words ▾

Uses For temporary relief of itchy, dry skin, redness and inflammation

⏱️ Dosage and Administration 12 words ▾

Directions Apply generously to affected areas up to 4 times a day

⚠️ Warnings 31 words ▾

Warnings • For external use only • Avoid contact with eyes Keep out of reach of children • If symptoms persist for more than 7 days or worsen, consult your physician

🧪 Active Ingredient 36 words ▾

Active ingredients (in gel) Sulphur 1X HPUS Graphites 3X HPUS Mezereum 6X HPUS Rhus tox 6X HPUS Purpose For dry, scaly, itchy skin For eczema; dry, rough skin For eczema For dermatitis; red, inflamed, itchy skin

🧪 Inactive Ingredients 97 words ▾

Inactive ingredients Achillea Millefolium Extract, Alcohol, Aloe Barbadensis Leaf Extract, Benzoic Acid, Beta-Glucan, C13-14 Isoparaffin, Calendula Officinalis Flower Extract, Carbomer, Chamomilla Recutita (Matricaria) Flower Extract, Citrus Aurantium Dulcis (Orange) Flower Extract, Echinacea Angustifolia Extract, Ethyl Linoleate, Foeniculum Vulgare (Fennel) Seed Extract, Geranium Maculatum Extract, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, lnulin, Laureth-7, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methyl Salicylate, Oleyl Lactate, Phenoxyethanol, Polyacrylamide, Potassium Sorbate, Propylene Glycol, Rosa Canina Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Sambucus Nigra Flower Extract, Sodium Benzoate, Sodium Hydroxide, Sorbic Acid, Tocopheryl Acetate, Water (Aqua), Yogurt Powder

🎯 Purpose 19 words ▾

Purpose For dry, scaly, itchy skin For eczema; dry, rough skin For eczema For dermatitis; red, inflamed, itchy skin

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 43689-0022-02 · The 43689-0036-02 · The →
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.