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StellaLife VEGA Oral Care Gel 8 [hp_X]/mL; 30 [hp_X]/mL; 8 [hp_X]/mL; 18 [hp_X]/mL; 5 [hp_X]/mL; 12 [hp_X]/mL; 10 [hp_X]/mL Gel — NDC 61727-0117-01 package photo

StellaLife VEGA Oral Care Gel 8 [hp_X]/mL; 30 [hp_X]/mL; 8 [hp_X]/mL; 18 [hp_X]/mL; 5 [hp_X]/mL; 12 [hp_X]/mL; 10 [hp_X]/mL Gel

by Homeocare Laboratories, Inc. · 1 BOTTLE, PUMP in 1 BOX (61727-117-01) / 30 mL in 1 BOTTLE, PUMP
NDC 61727-0117-01
🏷️ FDA NDC (as labeled) 61727-117-01 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) 61727-117-01
Product NDC 61727-117
11-digit billing NDC 61727011701
UNII 1NM3M2487K, N94C2U587S, G0R4UBI2ZZ, O80TY208ZW, XK4IUX8MNB, 877L01IZ0P +6 more
SPL Set ID b701234a-0bd2-16d3-e053-2995a90a5b13
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-01-08
Route DENTAL, TOPICAL
Dosage form GEL
Substance CALCIUM SULFIDE; STRYCHNOS IGNATII SEED; DELPHINIUM STAPHISAGRIA SEED; ARNICA MONTANA; MATRICARIA RECUTITA; RUTA GRAVEOLENS FLOWERING TOP; HYPERICUM PERFORATUM; ECHINACEA ANGUSTIFOLIA; SILICON DIOXIDE; ECHINACEA PURPUREA; LEDUM PALUSTRE TWIG; CALENDULA OF
Why two NDCs? The FDA registers this code as 61727-117-01 — 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 → 61727-0117-01. 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

LabelerHomeocare Laboratories, Inc.
Labeler code61727
First marketedJan 2021
Product typeHuman Otc Drug
Portfolio10 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?

StellaLife VEGA Oral Care Gel is a topical dental gel marketed as a homeopathic product. It contains multiple plant and mineral ingredients, including arnica montana, calendula, echinacea species, hypericum, and matricaria, which are traditionally used in homeopathic practice for oral comfort and healing support. This product is not evaluated by the FDA for effectiveness and is marketed based on homeopathic tradition rather than clinical evidence.

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
FlavorPeppermint
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 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII R33S7TK2EP
    Hydroxyethyl cellulose is a thickening agent made from processed plant cellulose. It's used in medicines to increase viscosity, improve texture, and help distribute active ingredients evenly throughout liquid or semi-solid formulations.
  • UNII AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • 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 VCQ006KQ1E
    Xylitol is a naturally occurring sugar alcohol derived from plants. It's used in medicines as a sweetener, bulking agent, and to improve taste, especially in liquid formulations and chewable tablets.

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

The official label also statesCitric acid, Glycerin, Potassium sorbate, Purified water. Allantoin, Hydroxyethylcellulose, Peppermint oil, Purified water, Sodium benzoate, Xylitol Allantoin, Citric acid, Glycerin, Peppermint flavor, Peppermint oil, Polysorbate 20, Potassium sorbate, Propolis, Purified water, Xylitol

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
StellaLife VEGA Oral Care Gel 8 [hp_X]/mL; 30 [hp_X]/mL; 8 [hp_X]/mL; 18 [hp_X]/mL; 5 [hp_X]/mL; 12 [hp_X]/mL; 10 [hp_X]/mLthis 61727-0117-01 Homeocare 1 bottle — — 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

🏛️
2021
On the market since
Jan 2021
📍
2026
Currently FDA-listed
5 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 StellaLife VEGA Oral Care Gel (this brand).

Top reported reactions

Therapeutic Response Decreased1

Reporter sex

0 reports
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
61727-0117-01 You're viewing this 1 BOTTLE, PUMP in 1 BOX (61727-117-01) / 30 mL in 1 BOTTLE, PUMP 2021-01-08 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

StellaLife VEGA Oral Care Gel 8 [hp_X]/mL; 30 [hp_X]/mL; 8 [hp_X]/mL; 18 [hp_X]/mL; 5 [hp_X]/mL; 12 [hp_X]/mL; 10 [hp_X]/mL GEL 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 61727-117-01, 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: 61727-0117-01, written without dashes as 61727011701. 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 61727-0117-01, the first segment (61727) is the labeler code FDA assigned to Homeocare Laboratories, Inc.; the middle segment (0117) 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 Homeocare Laboratories, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Homeocare Laboratories, 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 32 words ▾

Usage Pain and swelling relief Promotes Healing Reduces Bruising

Usage Promotes healing Reduces bruising Relieves oral ulcers Hydrates oral cavity

Uses Promotes oral health Hydrates oral cavity Supports healthy gums Freshens breath

⏱️ Dosage and Administration 171 words ▾

Directions Adults and children over 6 years of age: Shake well . Spray 4 times per application under the tongue . Repeat 3-4 times per dday 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 under 6 years of age.

Directions Adults and children ovver the age of 6 years: Shake well. Use 3/4 tablespoon (10 ml) per application 3 times a day. Swish in the mouth for 1-2 minutes abnd 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.

⚠️ Warnings ~1 min read ▾

Warnings Do not use if you have a known allergy or sensitivity to any of the following ingredients Stop use and consult a healthcare professional if you experience irritation or unusual sensitivity, or develop a rash. As with any drug, if you are pregnant or nursing a baby, seek the advise of a healthcare professional before using this product. Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek professional assistance or contact poison control center immediately. If pain, swelling or other related symptoms persist for more than 7 days of use, contact a dental professional.

Warnings Do not use if you have a known allergy or sensitivity to any of the following ingredients Stop use and consult a healthcare professional if you experience irritation or unusual sensitivity, or develop a rash. As with any drug, if you are pregnant or nursing a baby, seek the advise of a healthcare professional before using this product. Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek professional assistance or contact poison control center immediately. If pain, swelling or other related symptoms persist for more than 7 days of use, contact a dental professional.

Warnings Do not use if you have a known allergy or sensitivity to any of the following ingredients Stop use and consult a healthcare professional if you experience irritation or unusual sensitivity, or develop a rash. As with any drug, if you are pregnant or nursing a baby, seek the advise of a healthcare professional before using this product. Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek professional assistance or contact poison control center immediately. If pain, swelling or other related symptoms persist for more than 7 days of use, contact a dental professional.

🧪 Active Ingredient 154 words ▾

Drug Facts Contains 7.14% each of the following HPUS Ingredients Active Ingredients Purpose Arnica 3X, 6X, 18X Bruising, swelling Calendula 3X Antiseptic Chamomilla 5X Swelling Echinacea Angustifolia 3X Antiseptic Echinacea Purpurea 3X Antiseptic Hepar Sulph Calc 8X Antiseptic Hypericum 10X Bruising, wound healing Ignata 30X Soothing Ledum Palusttre 6X Analgesic, antiseptic Ruta 12X Bruising Silicea 8X Analgesic, antiseptic Staphysagria 8X Analgesic, soothing

Drug Facts Contains 0.0714% of each of the following HPUS ingredients: Active Ingredients Purpose Arnica 3X, 6X, 18X Bruising, swelling Calendula 3X Antiseptic Chamomilla 5X Swelling Echinacea angustifolia 3X Antiseptic Echinacea purpurea 3X Antiseptic Hepar sulph calc 8X Antiseptic Hypericum 10X Bruising, would healing Ignata 30X Soothing Ledum palustre 6X Analgesic Ruta 12X Bruising Silicea 8X Analgesic, antiseptic Staphysagria 8X Analgesic, soothing

Drug Facts Contains 0.55% of each of the following HPUS ingredients: Active Ingredient Purpose Azadirachta Indica 1X Antiginivitis, swelling Calendula 1X Antiseptic Echinacea Purpurea 1X Antiseptic Plantago Major 1X Antiseptic

🧪 Inactive Ingredients 38 words ▾

Inactive Ingredients Citric acid, Glycerin, Potassium sorbate, Purified water.

Inactive Ingredients Allantoin, Hydroxyethylcellulose, Peppermint oil, Purified water, Sodium benzoate, Xylitol

Inactive Ingredients Allantoin, Citric acid, Glycerin, Peppermint flavor, Peppermint oil, Polysorbate 20, Potassium sorbate, Propolis, Purified water, Xylitol

🎯 Purpose 39 words ▾

Uses Temporarily Relieves pain and swelling. Promotes healing. Reduces bruising.

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

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

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 61727-0115-01 · Homeocare 61727-0118-01 · Homeocare →
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.