NDC 51393-5622-03 — Eczema Control Centella Asiatica, Iris

🆔 Identity & classification

FDA NDC (as labeled) 51393-5622-3

Product NDC 51393-5622

11-digit billing NDC 51393562203

UNII 7M867G6T1U, X43D4L3DQC, 597E9BI3Z3, 451W47IQ8X, N94C2U587S, ETJ7Z6XBU4 +2 more

UPC 0830743011229

SPL Set ID aed6fd4d-2c78-4ea5-b24f-83993213cefe

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2011-12-01

Route TOPICAL

Dosage form SOLUTION/ DROPS

Substance CENTELLA ASIATICA WHOLE; IRIS VERSICOLOR ROOT; ARCTIUM LAPPA ROOT; SODIUM CHLORIDE; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE; TARAXACUM OFFICINALE; THUJA OCCIDENTALIS ROOT

Why two NDCs? The FDA registers this code as 51393-5622-3 — 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 → 51393-5622-03. 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

LabelerForces of Nature

Labeler code51393

First marketedDec 2011

Product typeHuman Otc Drug

Portfolio25 products on file

🔎 All NDCs from Forces of Nature

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 a homeopathic solution in drop form applied to the skin. It contains eight plant-derived and mineral ingredients including centella asiatica, burdock root (arctium lappa), iris versicolor, and thuja occidentalis, which are traditionally used in homeopathic practice for skin concerns. Homeopathic products are marketed based on traditional use rather than FDA evaluation for effectiveness. This product is not approved by the FDA and has not been tested for safety or effectiveness in the way conventional medicines are.

Patient education

📘 MedlinePlus patient leaflet ↗

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 9RES347CKG
A fragrant oil derived from lavandin plants, used as a flavoring and aromatic agent to improve the taste and smell of medicines.
UNII SA8AR2W4ER
A natural oil extracted from chamomile flower tops, used as a flavoring and fragrance agent to improve taste and aroma in medicines.
UNII D50IC2T8FU
Niaouli oil is a plant-derived essential oil used as a flavoring agent and fragrance component in medicines. It adds taste and aroma to make medications more palatable.
UNII 0J3G3O53ST
Palmarosa oil is a fragrant plant-derived oil used as a flavoring agent and fragrance in medications. It helps mask unpleasant tastes or odors in oral medicines and improves overall product appeal.
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.
UNII 8LGU7VM393
Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
UNII QX10HYY4QV
Sesame oil is a plant-derived oil from sesame seeds. It's used in medicines as a solvent or carrier to dissolve or suspend active ingredients, helping them mix evenly throughout the formulation.

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

The official label also statesGerman Chamomile Oil*, Lavandin Oil*, Niaouli Oil*, Palmarosa Oil*, Pine Oil*, Rosemary Oil*, Sesame Oil* *Certified organic

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 system	Per mL	Per 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: 5 ml 11 ml 33 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.

🔁 Therapeutic equivalents

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Eczema Control 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_X]/100mL; 12 [hp_C]/100mL; 6 [hp_X]/100mL; 6 [hp_Cthis 51393-5622-03	Forces	30 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

🏛️

2011

On the market since

Dec 2011

📍

2026

Currently FDA-listed

15 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 NDC	Description	Marketing start	Status
51393-5622-01	11 mL in 1 BOTTLE, DISPENSING (51393-5622-1)	2011-12-01	Active
51393-5622-02	33 mL in 1 BOTTLE, DISPENSING (51393-5622-2)	2011-12-01	Active
51393-5622-03 You're viewing this	30 mL in 1 BOTTLE, DROPPER (51393-5622-3)	2021-08-01	Active
51393-5622-05	5 mL in 1 BOTTLE, DISPENSING (51393-5622-5)	2016-07-01	Active

You're viewing one of 4 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 51393-5622-03?

NDC 51393-5622-03 contains 30 mL — 30 ml in 1 bottle, dropper.

What is the difference between NDC 51393-5622-03 and NDC 51393-5622-05?

Both are Eczema Control Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, and Thuja Occidentalis Root 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_X]/100mL; 12 [hp_C]/100mL; 6 [hp_X]/100mL; 6 [hp_C Solution/ Drops — the drug itself is identical. NDC 51393-5622-03 is the 30 mL package, while NDC 51393-5622-05 is the 5 ml package.

What NDC number is used to bill for this package of Eczema Control Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, and Thuja Occidentalis Root 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_X]/100mL; 12 [hp_C]/100mL; 6 [hp_X]/100mL; 6 [hp_C Solution/ Drops?

Bill NDC 51393-5622-03 — the 11-digit billing format is 51393562203. 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

Eczema Control Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, and Thuja Occidentalis Root 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_C]/100mL; 12 [hp_X]/100mL; 12 [hp_C]/100mL; 6 [hp_X]/100mL; 6 [hp_C SOLUTION/ DROPS 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 51393-5622-3, 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: 51393-5622-03, written without dashes as 51393562203. 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 51393-5622-03, the first segment (51393) is the labeler code FDA assigned to Forces of Nature; the middle segment (5622) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 Forces of Nature. 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 3 other package presentations of this same product, including 5 ml (51393-5622-05), 11 ml (51393-5622-01), 33 ml (51393-5622-02). 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?

Forces of Nature 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 20 words ▾

Uses for the temporary relief of itching associated with minor skin irritations and rashes which may be due to eczema.

⏱️ Dosage and Administration 19 words ▾

Directions shake well before use. Apply to affected area by gently rubbing into skin 3 to 4 times daily.

⚠️ Warnings 85 words ▾

Warnings For external use only. Some individuals may be sensitive to essential oils. Begin with a small drop to determine if product causes any irritation.

Discontinue use if any irritation occurs. Stop use and consult a doctor if condition worsens. Not for use on children under the age of 2 without physician direction.

Keep out of reach of children. If pregnant or breast-feeding, ask a health professional before use. If accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center.

📦 Storage and Handling 16 words ▾

Other information Keep in cool dark place store upright tighten cap after use to prevent oxidation

🧪 Active Ingredient 63 words ▾

Active ingredients Purpose Hydrocotyle asiatica USDA Certified Organic 12C Heals Thickened and Itchy Skin Horsetail (Source of Silica) 6X Reduces Inflammation Natrum muriaticum 12X Remedy for Eczema Iris versicolor 12C Relieves Itchy Skin associated with Eczema Lappa arctium 12C Remedy for Eczema Ruta graveolens 12C Relieves Itchy Skin Taraxacum officinale 6C Remedy for Skin Eruptions Thuja occidentalis 8X Relieves Skin Eruptions with Itching

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients Sesame Oil , Lavandin Oil , Palmarosa Oil , Pine Oil , Rosemary Oil , Niaouli Oil , German Chamomile Oil

🎯 Purpose 63 words ▾

Active ingredients Purpose Hydrocotyle asiatica USDA Certified Organic 12C Heals Thickened and Itchy Skin Horsetail (Source of Silica) 6X Reduces Inflammation Natrum muriaticum 12X Remedy for Eczema Iris versicolor 12C Relieves Itchy Skin associated with Eczema Lappa arctium 12C Remedy for Eczema Ruta graveolens 12C Relieves Itchy Skin Taraxacum officinale 6C Remedy for Skin Eruptions Thuja occidentalis 8X Relieves Skin Eruptions with Itching

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

🔗 Related NDC lookups

🧪 All Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, And Thuja Occidentalis Root NDCsSame ingredient 🏭 All Forces labeler NDCsLabeler code 51393