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Scar Control Calendula Officinalis Flowering Top, Allylthiourea, and Silicon Dioxide 6 [hp_X]/1000mL; 8 [hp_C]/1000mL; 6 [hp_X]/1000mL Solution/ Drops, 33 mL — NDC 51393-7112-02 package photo

Scar Control Calendula Officinalis Flowering Top, Allylthiourea, and Silicon Dioxide 6 [hp_X]/1000mL; 8 [hp_C]/1000mL; 6 [hp_X]/1000mL Solution/ Drops, 33 mL

by Forces of Nature · 33 mL in 1 BOTTLE, DISPENSING (51393-7112-2)
NDC 51393-7112-02
🏷️ FDA NDC (as labeled) 51393-7112-2 billing pads the package segment with a zero
This package
Contains33 mL Pack sizes4 compare ↓
Also comes in: 4 ml 51393-7112-04 11 ml 51393-7112-01 30 ml 51393-7112-03
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 51393-7112-2
Product NDC 51393-7112
11-digit billing NDC 51393711202
UNII 18E7415PXQ, 706IDJ14B7, ETJ7Z6XBU4
UPC 0830743009073
SPL Set ID 595c3423-6b52-48fc-8a95-00b53c1ecc7b
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2011-04-06
Route TOPICAL
Dosage form SOLUTION/ DROPS
Substance CALENDULA OFFICINALIS FLOWERING TOP; ALLYLTHIOUREA; SILICON DIOXIDE
Why two NDCs? The FDA registers this code as 51393-7112-2 — 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 → 51393-7112-02. 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 marketedApr 2011
Product typeHuman Otc Drug
Portfolio25 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?

Scar Control is an unapproved homeopathic topical solution applied as drops to the skin. It contains calendula officinalis flowering top, allylthiourea, and silicon dioxide in homeopathic dilutions. In homeopathic practice, these ingredients are traditionally used to address skin concerns and scarring, though homeopathic products are marketed based on traditional use and are not evaluated by the FDA 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.

💊 What it looks like

Color yellow
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 P62Y550X24
    A plant extract from helichrysum flowers that may be used as a natural fragrance, flavor enhancer, or colorant in medicines. It contributes aroma or taste to make the medication more pleasant.
  • 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 J99W255AWF
    A plant-derived oil from rosehip seeds used as an emollient and skin-conditioning agent. It helps soften the product and improve how it spreads on skin or mucous membranes.
  • 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.

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

The official label also statesHelichrysum Oil*, Lavandin Oil*, Rosehip Seed 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 systemPer mLPer 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: 4 ml 11 ml 30 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Scar Control 6 [hp_X]/1000mL; 8 [hp_C]/1000mL; 6 [hp_X]/1000mLthis 51393-7112-02 Forces 33 ml — — Discontinued —
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
Apr 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 NDCDescription Marketing startStatus
51393-7112-01 11 mL in 1 BOTTLE, DISPENSING (51393-7112-1) 2011-04-06 Active
51393-7112-02 You're viewing this 33 mL in 1 BOTTLE, DISPENSING (51393-7112-2) 2011-04-06 Discontinued by firm
51393-7112-03 30 mL in 1 BOTTLE, DISPENSING (51393-7112-3) 2021-06-01 Active
51393-7112-04 4 mL in 1 BOTTLE (51393-7112-4) 2016-10-01 Active

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

Pack size FAQ

What quantity is in NDC 51393-7112-02?
NDC 51393-7112-02 contains 33 mL — 33 ml in 1 bottle, dispensing.
What is the difference between NDC 51393-7112-02 and NDC 51393-7112-04?
Both are Scar Control Calendula Officinalis Flowering Top, Allylthiourea, and Silicon Dioxide 6 [hp_X]/1000mL; 8 [hp_C]/1000mL; 6 [hp_X]/1000mL Solution/ Drops — the drug itself is identical. NDC 51393-7112-02 is the 33 mL package, while NDC 51393-7112-04 is the 4 ml package.
What NDC number is used to bill for this package of Scar Control Calendula Officinalis Flowering Top, Allylthiourea, and Silicon Dioxide 6 [hp_X]/1000mL; 8 [hp_C]/1000mL; 6 [hp_X]/1000mL Solution/ Drops?
Bill NDC 51393-7112-02 — the 11-digit billing format is 51393711202. 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 No longer marketed (per FDA listing data)

About homeopathic listings

Scar Control Calendula Officinalis Flowering Top, Allylthiourea, and Silicon Dioxide 6 [hp_X]/1000mL; 8 [hp_C]/1000mL; 6 [hp_X]/1000mL 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 51393-7112-2, 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: 51393-7112-02, written without dashes as 51393711202. 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 51393-7112-02, the first segment (51393) is the labeler code FDA assigned to Forces of Nature; the middle segment (7112) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 4 ml (51393-7112-04), 11 ml (51393-7112-01), 30 ml (51393-7112-03). 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 6 words ▾

Uses To reduce and eliminate scars.

⏱️ Dosage and Administration 33 words ▾

Directions Shake well before use. For best results, begin using as soon as wound has healed. Roll a small amount onto the scar and gently massage into the skin.Apply 3 times per day.

⚠️ Warnings 110 words ▾

Warnings For external use only. Some individuals may be sensitive to essential oils.Begin with a small drop to determine if the product causes any increased redness or irritation and discontinue use if it irritates your skin.Avoid contact with eyes.If contact occurs, rinse eyes thoroughly with water.Not for use on children under the age of 2 without physician direction. If you are 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. Keep out of reach of children. If condition worsens or does not improve after regular use of this product as directed, consult a doctor.

🧪 Active Ingredient 30 words ▾

Active Ingredients Purpose Calendula Officinalis* 6X Promotes Healthy Skin and Healing Equisetum Arvense* 6X (Source of Silica) Remedy for Painful Scars, Keloids Thiosinaminimum* 8C For Dissolving Scar Tissue *Certified Organic

🧪 Inactive Ingredients 15 words ▾

Inactive Ingredients Helichrysum Oil*, Lavandin Oil*, Rosehip Seed Oil*, Rosemary Oil*, Sesame Oil* *Certified Organic

🎯 Purpose 30 words ▾

Active Ingredients Purpose Calendula Officinalis* 6X Promotes Healthy Skin and Healing Equisetum Arvense* 6X (Source of Silica) Remedy for Painful Scars, Keloids Thiosinaminimum* 8C For Dissolving Scar Tissue *Certified Organic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 51393-6989-01 · Forces 51393-7434-01 · Forces →
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.