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Dr. Talbots Vital 12 Calc fluor, Calc phos, Calc sulph, Ferrum phos, Kali mur, Kali phos, Kali sulph, Mag phos, Nat mur, Nat phos, Nat sulph, Silicea, Zinc gluc 3 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 1 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Tablet, Soluble, 140-count — NDC 70797-0233-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Dr. Talbots Vital 12 Calc fluor, Calc phos, Calc sulph, Ferrum phos, Kali mur, Kali phos, Kali sulph, Mag phos, Nat mur, Nat phos, Nat sulph, Silicea, Zinc gluc 3 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 1 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Tablet, Soluble, 140-count — NDC 70797-233-01 (Billing 70797-0233-01)

by Talbot's Pharmaceuticals Family Products, LLC · 1 BOTTLE in 1 CARTON / 140 TABLET, SOLUBLE in 1 BOTTLE

This is a package of 140 tablets of Dr. Talbots Vital 12 Calc fluor, Calc phos, Calc sulph, Ferrum phos, Kali mur, Kali phos, Kali sulph, Mag phos, Nat mur, Nat phos, Nat sulph, Silicea, Zinc gluc 3 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 1 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Tablet, Soluble from Talbot's Pharmaceuticals Family Products, LLC, marketed since Jul 2021 and currently FDA-listed. It is this product's only package size.

NDC 70797-0233-01
🏷️ FDA NDC (as labeled) 70797-233-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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

NDC database record

One package, one record: these facts belong to NDC 70797-233-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
70797 labeler · 233 product · 01 package
Package marketed since
Jul 1, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0370797233401
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70797-233-01
Product NDC 70797-233
11-digit billing NDC 70797023301
UNII 91D9GV0Z28, 451W47IQ8X, 70WT22SF4B, U6WSN5SQ1Z, O3B55K4YKI, 660YQ98I10 +7 more
UPC 0370797233401
SPL Set ID c10bb804-8169-63da-e053-2a95a90a8306
Established class (EPC) Blood Coagulation Factor; Calculi Dissolution Agent; Cations; Copper Absorption Inhibitor; Increased
Physiologic effect Decreased Copper Ion Absorption
Chemical class Calcium; Divalent
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-07-01
Route ORAL
Dosage form TABLET, SOLUBLE
Substance TRIBASIC CALCIUM PHOSPHATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; ZINC GLUCONATE; CALCIUM FLUORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SILICON DIOXIDE; CALCIUM SULFATE ANHYDROUS; FERROSOFERRIC PHOSPHATE; POTASSIUM SULFAT
Why two NDCs? The FDA registers this code as 70797-233-01 — 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 → 70797-0233-01. 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.

Clinical

🧪 What is this product?

Dr. Talbots Vital 12 is an unapproved homeopathic tablet taken by mouth. It contains twelve mineral salts (including forms of calcium, potassium, magnesium, sodium, iron, silicon, and zinc) that are used in homeopathic tradition. These ingredients are selected based on homeopathic practice rather than established medical uses. Homeopathic products are not evaluated by the FDA for safety or 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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
70797-0233-01 You're viewing this Main listing 1 BOTTLE in 1 CARTON / 140 TABLET, SOLUBLE in 1 BOTTLE 2021-07-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Dr. Talbots Vital 12 3 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 1 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]this 70797-0233-01 Talbot's 140 tablets — — 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
Jul 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.

What it looks like

Color purple
ShapeRound
Size5 mm
ScoringNot scored
FlavorBerry
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 Z4IFJ0AK1E
    A liquid extract from elderberry fruit used as a flavoring and coloring agent in medicines. It provides natural purple color and fruity taste to make the product more palatable.
  • UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • UNII EWQ57Q8I5X
    Lactose monohydrate is a natural sugar derived from milk. It serves as a filler and binder in tablets and capsules, helping create the proper size, texture, and consistency of the medicine.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • 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 statesInactive ingredients Elderberry Juice Powder, Hyaluronic Acid, Lactose, Magnesium Stearate, Maltodextrin, Microcrystalline, Cellulose, Xylitol. Contains lactose from milk.

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.

Manufacturer & labeler

LabelerTalbot's Pharmaceuticals Family Products, LLC
Labeler code70797
First marketedJul 2021
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from Talbot's Pharmaceuticals Family Products, LLC labeler code 70797

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.

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 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 29 words ▾

Provides a daily supply of Vital 12 cell salts to help balance and support overall cell functions. Provides zinc and elderberry to help with immune support.+ Indication & Usage

⏱️ Dosage and Administration 44 words ▾

Directions Infant Ages 3m - 1 year: 1 tablet Children Ages 2 - 6 years: 2 tablets Adults & Children Ages 7+ years: 4 tablets Dissolve under tongue 4 times a day. Tablets may be crushed or dissolved in a teaspoon of water. Directions

⚠️ Warnings 49 words ▾

Warnings Do not use if seal under cap is broken or missing. Consult physician before use if the child has medical condition or is taking any medication. Do not use more often than directed or if your child has a known allergy to any ingredient in this product. Warnings

🧪 Active Ingredient 74 words ▾

Active ingredients Equal amounts of: Calc fluor 6X HPUS, Calc phos 3X HPUS, Calc sulph 3X HPUS, Ferrum phos 3X HPUS, Kali mur 3X HPUS, Kali phos 3X HPUS, Kali sulph 3X HPUS, Mag phos 3X HPUS, Nat mur 6X HPUS, Nat phos 3X HPUS, Nat sulph 3X HPUS, Silicea 6X HPUS, Zinc gluc 1X HPUS "HPUS" indicates that the active ingredients are in the official Homeopathic Pharmacopeia of the United States. Active Ingredients

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients Elderberry Juice Powder, Hyaluronic Acid, Lactose, Magnesium Stearate, Maltodextrin, Microcrystalline, Cellulose, Xylitol. Contains lactose from milk. Inactive ingredients

🎯 Purpose 27 words ▾

Provides a daily supply of Vital 12 cell salts to help balance and support overall cell functions. Provides zinc and elderberry to help with immune support.+ Uses

📄 Stop Use and Ask a Doctor If 14 words ▾

Stop use and ask a doctor if irritation, swelling, or rash develops. Stop use

📄 Keep Out of Reach of Children 29 words ▾

Keep out of reach of children. In case of overdose or allergic reaction, get medical help or contact a Poison Control Center immediately. Keep out of reach of children

📄 Other Information 23 words ▾

Other information Do not use if seal under cap is broken or missing. Store tablets in dry conditions at room temperature. Other information

📄 Questions or Comments 28 words ▾

Questions or comments? Call us at 1-855-366-7755 (U.S.A. only) M-F 8AM-5PM CST +Claims based on traditional homeopathic practices, not accepted medical evidence. Not FDA evaluated. Questions or comments

📄 Package Label / Principal Display Panel 1 words ▾

PDP

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

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Dr. Talbots Vital 12 Calc fluor, Calc phos, Calc sulph, Ferrum phos, Kali mur, Kali phos, Kali sulph, Mag phos, Nat mur, Nat phos, Nat sulph, Silicea, Zinc gluc 3 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 1 [hp_X]/1; 6 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 TABLET, SOLUBLE 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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Talbot's Pharmaceuticals Family Products, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Talbot's Pharmaceuticals Family Products, 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.
← 70797-0160-01 · Talbots 70797-0240-01 · Talbot's →
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.