Home › NDC Lookup › Ingredients › Kit › 69685-0107-01
Vega Oral Care Recovery Spearmint Kit Kit, 1 kit — NDC 69685-0107-01 package photo

Vega Oral Care Recovery Spearmint Kit Kit, 1 kit

by StellaLife, Inc. · 1 KIT in 1 BOX (69685-107-01)
NDC 69685-0107-01
🏷️ FDA NDC (as labeled) 69685-107-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 69685-107-01
Product NDC 69685-107
11-digit billing NDC 69685010701
SPL Set ID 148ca440-5fe0-afea-e063-6394a90aea0d
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-02-08
Route ORAL, TOPICAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 69685-107-01 — 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 → 69685-0107-01. 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

LabelerStellaLife, Inc.
Labeler code69685
First marketedFeb 2024
Product typeHuman Otc Drug
Portfolio17 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?

Vega Oral Care Recovery Spearmint Kit is a homeopathic product supplied as a kit for oral and topical use. Homeopathic products are marketed based on traditional homeopathic use and are not evaluated by the FDA for effectiveness. This kit contains homeopathic ingredients that are traditionally used in homeopathic practice, though their specific active components are not listed on this directory entry. Homeopathic oral care products of this type are typically associated with mouth and throat comfort in homeopathic tradition.

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.

From the label’s inactive-ingredient sectionAlcohol, Allantoin, Citric acid, Cucumber flavor, Glycerin, Potassium sorbate, Propolis, Purified water, Sodium benzoate, Xylitol. Allantoin, Hydroxyethylcellulose, Potassium sorbate, Purified water, Sodium benzoate, Sodium metabisulfite, Xylitol.

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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
Vega Oral Care Recovery Spearmintthis 69685-0107-01 StellaLife, 1 kit — — FDA listed —
Vega Oral Care Recovery Peppermint 69685-0125-01 StellaLife, 1 kit — — FDA listed —
Vega Oral Care Recovery Cucumber 69685-0106-01 StellaLife, 1 kit — — 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

🏛️
2024
On the market since
Feb 2024
📍
2026
Currently FDA-listed
2 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Vega Oral Care Recovery Spearmint (this brand).

Top reported reactions

Blood Urine Present1
Neutrophil Count Decreased1

Reporter sex

0 reports
Female · 100%
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
69685-0107-01 You're viewing this 1 KIT in 1 BOX (69685-107-01) 2024-02-10 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing Kit / multi-component package

About homeopathic listings

Vega Oral Care Recovery Spearmint Kit KIT 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.

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 69685-107-01, 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: 69685-0107-01, written without dashes as 69685010701. 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 69685-0107-01, the first segment (69685) is the labeler code FDA assigned to StellaLife, Inc.; the middle segment (0107) 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 StellaLife, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
StellaLife, 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 47 words ▾

Uses ■ Antimicrobial. ■ Promotes oral health. ■ Hydrates oral cavity. ■ Supports healthy gums. ■ Freshens breath.

Unflavored Spray Uses ■ Relieves pain and swelling. ■ Promotes healing. ■ Reducing bruising.

Uses Temporarily Relieves pain and swelling. Promotes healing. Reduces bruising. Relieves oral ulcers. Hydrates oral

⏱️ Dosage and Administration 176 words ▾

Directions Adults and children over the age of 6 years: Shake well. Use 3/4 tablespoon (10 ml) per application 3 times a day or as recommended by a dental professional. Swish in the mouth for 1-2 minutes and then spit out. Do not swallow. Refrain from eating or drinking for at least 20 minutes after use. Consult your healthcare professional for use in children under 6 years of age.

Directions Adults and children over 6 years of age: Shake well. Spray 3-4 times per application under the tongue. Repeat 3-4 times per day or as directed by your doctor. Consult a healthcare professional for use in children under 6 years of age.

Directions Adults and children over the age of 6 years: Wash hands. Apply to the gum at the surgical or affected area with a cotton swab. Allow gel to dissolve. Do not eat or drink for 20 minutes after application. Apply 4 times per day or as directed by a dental professional. Consult your healthcare professional for use in children under6 years of age.

⚠️ Warnings 69 words ▾

Warnings For your protection, this bottle has an inner seal under the cap. Do not use if tamper evident cap seal is broken or missing.

Warnings For your protection, this bottle has a full body seal. Do not use if this tamper evident seal is broken or missing.

Warnings For your protection this container has a seal. Do not use if this tamper evident seal is broken or missing.

🧪 Active Ingredient 79 words ▾

Cucumber Rinse Active Ingredient Azadirachta indica 3X Calendula 3X Echinacea purpurea 3X Plantago major 3X

Unflavored Spray Active Ingredients Arnica 3X, 6X, 18X, Calendula 3X, Chamomilla 5X, Echinacea angustifolia 3X, Echinacea purpurea 3X, Hepar sulph calc 8X, Hypericum 10X, lgnatia 30X, Ruta 12X, Silicea 8X, Staphysagria 8X

Unflavored Gel Active Ingredients Arnica 3X, 6X, 18X, Calendula 3X, Chamomilla 5X, Echinacea angustifolia 3X, Echinacea purpurea 3X, Hepar sulph calc 8X, Hypericum 10X, lgnatia 30X, Ruta 12X, Silicea 8X, Staphysagria 8X

🧪 Inactive Ingredients 28 words ▾

Alcohol, Allantoin, Citric acid, Cucumber flavor, Glycerin, Potassium sorbate, Propolis, Purified water, Sodium benzoate, Xylitol.

Inactive Ingredients Allantoin, Hydroxyethylcellulose, Potassium sorbate, Purified water, Sodium benzoate, Sodium metabisulfite, Xylitol.

🎯 Purpose 92 words ▾

Purpose Active ingredient Purpose Azadirachta indica Antigingivitis, swelling Calendula Antiseptic Echinacea purpurea Antiseptic Plantago major Antiseptic

Purpose Active Ingredient Purpose Arnica Bruising, swelling Calendula Antiseptic Chamomilla Swelling Echinacea angustifolia Antiseptic Echinacea purpurea Antiseptic Hepar sulph calc Antiseptic Hypericum Bruising, wound healing lgnatia Soothing Ledum palustre Analgesic Ruta Bruising Silicea Analgesic, antiseptic Staphysagria Analgesic, soothing

Purpose Active Ingredient Purpose Arnica Bruising, swelling Calendula Antiseptic Chamomilla Swelling Echinacea angustifolia Antiseptic Echinacea purpurea Antiseptic Hepar sulph calc Antiseptic Hypericum Bruising, wound healing lgnatia Soothing Ledum palustre Analgesic Ruta Bruising Silicea Analgesic, antiseptic Staphysagria Analgesic, soothing

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 69685-0106-01 · StellaLife, 69685-0111-01 · StellaLife, →
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.