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Walgreens Pain Relieving Foot Pain Relief Apis Mellifera, Gelsemium Sempervirens Whole, and Pseudognaphalium Luteoalbum Leaf 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/g Cream — NDC 00363-9379-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Walgreens Pain Relieving Foot Pain Relief Apis Mellifera, Gelsemium Sempervirens Whole, and Pseudognaphalium Luteoalbum Leaf 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/g Cream — NDC 0363-9379-01 (Billing 00363-9379-01)

by Walgreen Company · 1 JAR in 1 CARTON / 113 g in 1 JAR

This is a package of Walgreens Pain Relieving Foot Pain Relief Apis Mellifera, Gelsemium Sempervirens Whole, and Pseudognaphalium Luteoalbum Leaf 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/g Cream from Walgreen Company, marketed since Feb 2023 and currently FDA-listed. It is this product's only package size.

NDC 00363-9379-01
🏷️ FDA NDC (as labeled) 0363-9379-01 billing pads the labeler segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 0363-9379-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0363 labeler · 9379 product · 01 package
Package marketed since
Feb 15, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 0363937901 2
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0363-9379-01
Product NDC 0363-9379
11-digit billing NDC 00363937901
UNII 7S82P3R43Z, R0519OZO3K, BGI20Z6M57
SPL Set ID 6c6cbae1-e2a9-43bf-9bfc-a20e9d22cc58
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 2023-02-15
Route TOPICAL
Dosage form CREAM
Substance APIS MELLIFERA; GELSEMIUM SEMPERVIRENS WHOLE; PSEUDOGNAPHALIUM LUTEOALBUM LEAF
Why two NDCs? The FDA registers this code as 0363-9379-01 — a 4-4-2 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 labeler segment → 00363-9379-01. 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 an unapproved homeopathic cream applied to the skin for foot pain relief. It contains three plant and insect-derived ingredients: Apis mellifera (honeybee), Gelsemium sempervirens (yellow jasmine), and Pseudognaphalium luteoalbum (cudweed). In homeopathic practice, these substances are traditionally used to address pain and inflammation. Homeopathic products are marketed based on historical use and tradition; the FDA does not evaluate them 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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
00363-9379-01 You're viewing this Main listing 1 JAR in 1 CARTON / 113 g in 1 JAR 2023-02-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Walgreens Pain Relieving Foot Pain Relief 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/gthis 00363-9379-01 Walgreen 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

🏛️
2023
On the market since
Feb 2023
📍
2026
Currently FDA-listed
3 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.

What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 WR1WPI7EW8
    A synthetic form of vitamin E used as an antioxidant. It prevents oils and fats in the medicine from breaking down and becoming rancid, helping keep the product stable during storage.
  • UNII 39W1PKE3JI
    Bergamot oil is a citrus extract from bergamot orange peel. It's used as a flavoring and fragrance agent to improve taste and aroma in medicines.
  • UNII 5TJD82A1ET
    A cooling crystalline substance made synthetically that is added to medicines as a fragrance, flavoring agent, and mild local irritant to produce a cooling or warming sensation on the skin or mucous membranes.
  • UNII 331KBJ17RK
    Canola oil is a plant-based oil derived from rapeseed. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients, and may improve how the body absorbs certain medications.
  • 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 I835H2IHHX
    A waxy substance derived from plant oils, used as an emulsifier and solubilizer to help mix oil and water ingredients together and keep them blended throughout the product's shelf life.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII EG3PA2K3K5
    Ethylhexyl stearate is a waxy oil made from stearic acid and ethylhexyl alcohol. In medicines, it acts as an emollient and thickener to improve texture and help the product spread smoothly on skin or dissolve properly.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • 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 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 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 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 YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • UNII OT38R0N74H
    PEG-75 stearate is a synthetic compound made by combining polyethylene glycol with stearic acid. It acts as an emulsifier and surfactant to help mix oils and water in the medicine and improve how the product dissolves and absorbs in the body.
  • 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 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 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 FD0913P475
    Steareth-10 is a synthetic compound made by combining stearic acid (a fatty substance) with polyethylene glycol. It works as an emulsifier and solubilizer in medications, helping to blend oil and water-based ingredients together and improve how drugs dissolve and absorb in the body.
  • UNII L0Q8IK9E08
    A synthetic compound made from stearic acid and polyethylene glycol. It acts as an emulsifier and solubilizer, helping mix oil and water-based ingredients and keeping them blended throughout the medicine's shelf life.
  • UNII 53J3F32P58
    A synthetic detergent derived from stearic acid, a fatty substance. It helps dissolve or distribute oil-based ingredients evenly throughout the medicine, acting as an emulsifier and solubilizer in tablets and capsules.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
  • 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.

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

The official label also statesbeeswax, camphor, canola oil, carbomer, ceteth-20, cetyl alcohol, citrus bergamia (bergamot) oil, ethylhexylglycerin, ethylhexyl stearate, eucalyptus globulus leaf oil, glyceryl stearate, menthol, methyl salicylate, PEG-75 stearate, PEG-100 stearate, phenoxyethanol, propylene glycol, sodium hydroxide, steareth-10, steareth-20, steareth-21, stearic acid, tocopheryl acetate, water, xanthan gum.

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

LabelerWalgreen Company
Labeler code00363
First marketedFeb 2023
Product typeHuman Otc Drug
Portfolio468 products on file

More NDCs from Walgreen Company labeler code 00363

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 60 words ▾

Use This product is a homeopathic remedy. As such, it has not undergone review or approval by the FDA and therefor has not been demonstrated to be safe or effective to diagnose, treat, prevent, mitigate or cure any condition or disease. According to homeopathic principles, the active ingredients in this product help temporarily relieve symptoms such as minor foot pain.

⏱️ Dosage and Administration 44 words ▾

Directions For Aduts and children 2 years of age and older: apply generous amount and massage into all surfaces of the feet, heels and toes. apply up to twice daily apply to legs as needed most beneficial when applied after bathing and drying feet.

⚠️ Warnings 141 words ▾

Warnings For external use only Do not use on damaged skin, open wounds, or mucous membranes According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms). Avoid contact with the eyes Do not use if you are allergic to Apis mellifica, Gelsenium sempervirens, Gmaphalium or any of this product's inactive ingredients. Do not bandage tightly Do not use with heating pads or other heating devices.

When using this product avoid contact with eyes. If pregnant, trying to get pregnant or breast-feeding , ask a health professional before use. Stop use and ask a doctor if conditions worsen or if symptoms persist for more than 72 hours or clear up and occur again within a few days.

Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📦 Storage and Handling 14 words ▾

Other information Active ingredients are manufactured according to homeopathic principles. Store at room temperature.

🧪 Active Ingredient 50 words ▾

Active ingredients C, K, CK and X are homeopathic dilutions. Purpose Apis mellifica 3X HPUS Pain Relief Gelsemium sempervirens 6X HPUS Pain Relief Gnaphalium 6X HPUS Pain Relief The letters 'HPUS' indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

🧪 Inactive Ingredients 45 words ▾

Inactive ingredients beeswax, camphor, canola oil, carbomer, ceteth-20, cetyl alcohol, citrus bergamia (bergamot) oil, ethylhexylglycerin, ethylhexyl stearate, eucalyptus globulus leaf oil, glyceryl stearate, menthol, methyl salicylate, PEG-75 stearate, PEG-100 stearate, phenoxyethanol, propylene glycol, sodium hydroxide, steareth-10, steareth-20, steareth-21, stearic acid, tocopheryl acetate, water, xanthan gum.

🎯 Purpose 50 words ▾

Active ingredients C, K, CK and X are homeopathic dilutions. Purpose Apis mellifica 3X HPUS Pain Relief Gelsemium sempervirens 6X HPUS Pain Relief Gnaphalium 6X HPUS Pain Relief The letters 'HPUS' indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

📄 Do Not Use 64 words ▾

Do not use on damaged skin, open wounds, or mucous membranes According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms). Avoid contact with the eyes Do not use if you are allergic to Apis mellifica, Gelsenium sempervirens, Gmaphalium or any of this product's inactive ingredients. Do not bandage tightly Do not use with heating pads or other heating devices.

📄 When Using This Product 8 words ▾

When using this product avoid contact with eyes.

📄 Stop Use and Ask a Doctor If 28 words ▾

Stop use and ask a doctor if conditions worsen or if symptoms persist for more than 72 hours or clear up and occur again within a few days.

🤰 If Pregnant or Breast-Feeding 15 words ▾

If pregnant, trying to get pregnant or breast-feeding , ask a health professional before use.

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-925-4733

📄 Package Label / Principal Display Panel 72 words ▾

PRINCIPAL DISPLAY PANEL - 113 g Jar Carton Walgreens Compare to the active ingredients in Magnilife ® Pain Relieving Foot Cream †† • WALGREENS • PHARMACIST RECOMMENDED † HOMEOPATHIC* Pain Relieving Foot Cream* APIS MELLIFICA 3X HPUS GELSEMIUM SEMPERVIRENS 6X HPUS GNAPHALIUM 6X HPUS Dye Free No Added Fragrance Moisturizing Helps with tingling, shooting pains, itching & sensitivity* NET WT 4 OZ (113 g) PRINCIPAL DISPLAY PANEL - 113 g Jar Carton

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

Walgreens Pain Relieving Foot Pain Relief Apis Mellifera, Gelsemium Sempervirens Whole, and Pseudognaphalium Luteoalbum Leaf 3 [hp_X]/g; 6 [hp_X]/g; 6 [hp_X]/g CREAM 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 Walgreen Company. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Walgreen Company 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.
← 00363-9369-31 · Walgreens 00363-9390-10 · Walgreen →
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.