Home › NDC Lookup › Ingredients › Calendula Officinalis, Chamomilla, Sepia... › 70105-0001-05
Natural Relief Patch for MOTION SICKNESS Calendula Officinalis, Chamomilla, Sepia, Tabacum, Cocculus Indicus, Nux Vomica 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C]/1 Patch, 5 patches — NDC 70105-0001-05 package photo

Natural Relief Patch for MOTION SICKNESS Calendula Officinalis, Chamomilla, Sepia, Tabacum, Cocculus Indicus, Nux Vomica 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C]/1 Patch, 5 patches

by Centered Enterprises, LLC · 5 PATCH in 1 BOX (70105-001-05)
NDC 70105-0001-05
🏷️ FDA NDC (as labeled) 70105-001-05 billing pads the product 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) 70105-001-05
Product NDC 70105-001
11-digit billing NDC 70105000105
UNII 18E7415PXQ, G0R4UBI2ZZ, QDL83WN8C2, 6YR2608RSU, 810258W28U, 269XH13919
UPC 0867676000105
SPL Set ID 161ed609-6029-4e2e-a480-5b4c72defa7b
Established class (EPC) Non-Standardized Plant Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Plant Proteins; Seed Storage Proteins
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-12-14
Route TOPICAL
Dosage form PATCH
Substance CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; SEPIA OFFICINALIS JUICE; TOBACCO LEAF; ANAMIRTA COCCULUS SEED; STRYCHNOS NUX-VOMICA SEED
Why two NDCs? The FDA registers this code as 70105-001-05 — 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 → 70105-0001-05. 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

LabelerCentered Enterprises, LLC
Labeler code70105
First marketedDec 2015
Product typeHuman Otc Drug
Portfolio6 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?

This is an unapproved homeopathic patch applied to the skin, containing plant-derived ingredients traditionally used in homeopathic practice for motion sickness symptoms. The formula includes calendula, chamomilla, sepia, tobacco leaf, cocculus, and nux vomica in homeopathic dilutions. Homeopathic products are marketed based on traditional use rather than clinical evidence, and the FDA does not evaluate them for effectiveness or safety in the same way as standard drugs.

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 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 32K497ZK2U
    Polyvinyl acetate is a synthetic plastic polymer derived from vinyl acetate. It acts as a binder and film-forming agent in medicines, helping to hold ingredients together and create protective coatings on tablets or capsules.
  • 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 Acrylic adhesive

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 eachPer 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
AnxiousRelief 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C] 70105-0004-05 Centered 6 patches — — FDA listed —
GoPatch Motion Sickness and Dizziness Relief 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C] 70105-0003-05 Centered 5 patches — — FDA listed —
GoPatch TummyRelief 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C] 70105-0005-05 Centered 5 patches — — FDA listed —
GoPatch HangoverRelief 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C] 70105-0006-05 Centered 6 patches — — FDA listed —
Natural Relief Patch for MOTION SICKNESS 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C]this 70105-0001-05 Centered 5 patches — — 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

🏛️
2015
On the market since
Dec 2015
📍
2026
Currently FDA-listed
11 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
70105-0001-05 You're viewing this 5 PATCH in 1 BOX (70105-001-05) 2015-12-14 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Natural Relief Patch for MOTION SICKNESS Calendula Officinalis, Chamomilla, Sepia, Tabacum, Cocculus Indicus, Nux Vomica 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_C]/1; 6 [hp_C]/1; 15 [hp_C]/1; 15 [hp_C]/1 PATCH 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 70105-001-05, 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: 70105-0001-05, written without dashes as 70105000105. 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 70105-0001-05, the first segment (70105) is the labeler code FDA assigned to Centered Enterprises, LLC; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (05) 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 Centered Enterprises, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Centered Enterprises, 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 31 words ▾

Uses* Temporarily relieves symptoms of dizziness and nausea aggrevated by or associated with motion. Useful for sea, car, and air sickness as well as motion sickness induced by amusement park rides.

⏱️ Dosage and Administration 76 words ▾

Directions For best results apply GoPatch before engaging in activities which promote motion sickness. GoPatch can also be used after motion sickness has already started. GoPatch must completely cover the navel.

Skin around nevel needs to be clean, dry and free of lotions. Remove white backing from one side of GoPatch. Smooth over half of navel.

Remove other half of white backing, smooth remainder over navel. Remove GoPatch no more than 12 hours after application .

⚠️ Warnings 75 words ▾

Warnings For external use only. Do not apply to broken or irritated skin. If skin sensitivity occurs, discontinue use . If you have extremely sensitive skin or have had reactions to other adhesives do not use this product . Ask a doctor before use: if pregnant or nursing; In children under 4 years of age. Consult a physician if symptoms persist for more than 7 days or worsen. Keep out of the reach of children.

🧪 Active Ingredient 70 words ▾

Active ingredients Purpose* Calendula Officinalis 3X HPUS soothes skin Chamomilla 3X HPUS calm sensitive skin Sepia 3C HPUS relieves dizziness & nausea accompanies by headache Tabacum 6C HPUS relieves vomiting, headache with nausea Cocculus Indicus 15C HPUS relieves nausea, vomiting, dizziness Nux Vomica 15C HPUS relieves nausea, stomach upset The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

🧪 Inactive Ingredients 4 words ▾

Inactive ingredients Acrylic adhesive

🎯 Purpose 30 words ▾

Temporarily relieves symptoms of dizziness and nausea aggrevated by or associated with motion. Useful for sea, car, and air sickness as well as motion sickness induced by amusement park rides.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 70101-0002-01 · Gas 70105-0002-05 · Centered →
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.