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Floriva VITAMIN A ACETATE, .BETA.-CAROTENE, Ascorbic acid, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, and SODIUM FLUORIDE 1000 [iU]/1; 1000 [iU]/1; 75 mg; 600 [iU]/1; 20 [iU]/1; 1.3 mg; 1.5 mg; 15 mg; 1.8 mg; 162 ug Tablet, Chewable, 1 tablet — NDC 52796-0174-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Floriva VITAMIN A ACETATE, .BETA.-CAROTENE, Ascorbic acid, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, and SODIUM FLUORIDE 1000 [iU]/1; 1000 [iU]/1; 75 mg; 600 [iU]/1; 20 [iU]/1; 1.3 mg; 1.5 mg; 15 mg; 1.8 mg; 162 ug Tablet, Chewable, 1 tablet — NDC 52796-174-01 (Billing 52796-0174-01)

by BonGeo Pharmaceuticals, Inc. · 1 BLISTER PACK in 1 CARTON / 1 TABLET, CHEWABLE in 1 BLISTER PACK

This is a package of 1 tablet of Floriva VITAMIN A ACETATE, .BETA.-CAROTENE, Ascorbic acid, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, and SODIUM FLUORIDE 1000 [iU]/1; 1000 [iU]/1; 75 mg; 600 [iU]/1; 20 [iU]/1; 1.3 mg; 1.5 mg; 15 mg; 1.8 mg; 162 ug Tablet, Chewable from BonGeo Pharmaceuticals, Inc., marketed since Oct 2014 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 52796-0174-01
🏷️ FDA NDC (as labeled) 52796-174-01 billing pads the product segment with a zero
This package
Contains1 tablet Pack sizes2 compare ↓
Main listing for product 52796-174 · Also comes in: 90 tablets 52796-174-90
Rx only On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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 52796-174-01 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
52796 labeler · 174 product · 01 package
Package marketed since
Oct 15, 2014
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0352796174909
FDA record last changed
Oct 1, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 52796-174-01
Product NDC 52796-174
11-digit billing NDC 52796017401
UNII 3LE3D9D6OY, 01YAE03M7J, PQ6CK8PD0R, 1C6V77QF41, H4N855PNZ1, X66NSO3N35 +10 more
UPC 0352796174909
SPL Set ID 34b2924f-d220-4344-8cdd-e7dda54061c2
Established class (EPC) Vitamin C; Vitamin D; Vitamin B6 Analog; Vitamin B12
Chemical class Ascorbic Acid; Vitamin D; Vitamin B 6; Analogs/Derivatives; Vitamin B 12
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-10-15
Route ORAL
Dosage form TABLET, CHEWABLE
Substance VITAMIN A ACETATE; BETA CAROTENE; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL; THIAMINE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE; LEVOMEFOLATE GLUCOSAMINE; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; ZINC GLUCONATE; CUPRIC OXIDE; SODIUM FLUORIDE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 78460000000515
GPI class Floriva
GCN Seq No 073063
GCN 37386
HICL code 041545
Ingredient (HICL) Pedi Multivit No.85/Fluoride
HIC1 code C
Therapeutic class — broad (HIC1) Electrolyte Balance/Metabolism/Nutrition
HIC2 code C6
Therapeutic class — intermediate (HIC2) Vitamins
HIC3 code C6H
Therapeutic class — specific (HIC3) Pediatric Vitamin Preparations
AHFS code 88:28.00.00
AHFS class Multivitamin Preparations
FDB label name FLORIVA 0.5 MG CHEWABLE TABLET
FDB brand name Floriva
Legend status Q — Non-drug — dietary supplement, vitamin, medical food, or herbal preparation
Quick answers
  • GSN (GCN sequence number): 073063
  • GCN: 37386
  • GPI-14 (Medi-Span): 78460000000515
  • HICL (First Databank): 041545
  • AHFS class code: 88:28.00.00
Why two NDCs? The FDA registers this code as 52796-174-01 — 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 → 52796-0174-01. 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

Label name FLORIVA 0.5 MG CHEWABLE TABLET Ingredient Pedi Multivit No.85/Fluoride
🧪 What is this product?

Floriva is a chewable tablet containing multiple vitamins and minerals taken by mouth. The product includes vitamins A, C, D, and E along with B-complex vitamins (thiamine, riboflavin, niacinamide, pyridoxine, folic acid, and cyanocobalamin) and biotin, which are typically used to supplement dietary intake of these nutrients. It also contains zinc and copper, which function as mineral supplements, and sodium fluoride, commonly included in products intended to support dental health. This product is marketed without an approved FDA application.

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.
Try another pack size: 90 tablets
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
52796-0174-01 You're viewing this Main listing 1 BLISTER PACK in 1 CARTON / 1 TABLET, CHEWABLE in 1 BLISTER PACK 2014-10-15 — Active
52796-0174-90 52796-174-90 90 TABLET, CHEWABLE in 1 BOTTLE 2014-10-15 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1 tablet — 1 blister pack in 1 carton / 1 tablet, chewable in 1 blister pack.
How does this package differ from NDC 52796-0174-90?
Both are Floriva VITAMIN A ACETATE, .BETA.-CAROTENE, Ascorbic acid, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, and SODIUM FLUORIDE 1000 [iU]/1; 1000 [iU]/1; 75 mg; 600 [iU]/1; 20 [iU]/1; 1.3 mg; 1.5 mg; 15 mg; 1.8 mg; 162 ug Tablet, Chewable — the drug itself is identical. This page's package is the 1 tablet one, while NDC 52796-0174-90 is the 90 tablets package.
What NDC number is used to bill for this package of Floriva VITAMIN A ACETATE, .BETA.-CAROTENE, Ascorbic acid, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, and SODIUM FLUORIDE 1000 [iU]/1; 1000 [iU]/1; 75 mg; 600 [iU]/1; 20 [iU]/1; 1.3 mg; 1.5 mg; 15 mg; 1.8 mg; 162 ug Tablet, Chewable?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Floriva 1000 [iU]/1; 1000 [iU]/1; 75 mg/1; 600 [iU]/1; 20 [iU]/1; 1.3 mg/1; 1.5 mg/1; 15 mg/1; 1.8 mg/1; 162 ugthis 52796-0174-01 BonGeo 1 tablet — — FDA listed —
Floriva 1000 [iU]/1; 1000 [iU]/1; 75 mg/1; 600 [iU]/1; 20 [iU]/1; 1.3 mg/1; 1.5 mg/1; 15 mg/1; 1.8 mg/1; 162 ug 52796-0173-12 BonGeo 1 tablet — — FDA listed —
Floriva 1000 [iU]/1; 1000 [iU]/1; 75 mg/1; 600 [iU]/1; 20 [iU]/1; 1.3 mg/1; 1.5 mg/1; 15 mg/1; 1.8 mg/1; 162 ug 52796-0177-90 BonGeo 90 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

🏛️
2014
On the market since
Oct 2014
📍
2026
Currently FDA-listed
12 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 White
ShapeHexagon (6 Sided)
Imprint174
Size13 mm
ScoringScored — splits in 2
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 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 96K6UQ3ZD4
    Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • 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.

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

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

LabelerBonGeo Pharmaceuticals, Inc.
Labeler code52796
First marketedOct 2014
Product typeHuman Prescription Drug
Portfolio4 products on file

More NDCs from BonGeo Pharmaceuticals, Inc. labeler code 52796

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.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 📋 Description 📄 Package Label / Principal Display Panel
⏱️ Dosage and Administration 7 words ▾

Directions USE AS DIRECTED BY YOUR PHYSICIAN.

⚠️ Warnings 49 words ▾

WARNING KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. IF OVERDOSAGE IS SUSPECTED, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY 1-800-222-1222. TABLET SHOULD BE CHEWED. THIS TABLET, AS WITH ALL TABLETS, IS NOT RECOMMENDED FOR CHILDREN UNDER AGE OF 4 DUE TO RISK OF CHOKING.

📦 Storage and Handling 86 words ▾

OTHER INFORMATION You may report serious side effects to 1-844-640-7607. Store in a cool, dry place at room temperature 20-25º Celsius (68-77º Fahrenheit) away from heat and sunlight. Store in original container.

The numeric identifier on this product's labeling is an assigned product code for use with pharmacy-level, health insurance and state level reimbursement programs and is not intended to denote registration with the FDA. The manufacturer of this product requires that it be dispensed only under the order of a physician or licensed medical practitioner.

📋 Description 22 words ▾

Description Off-white to pale yellow, speckled, berry flavored, hexagon shaped chewable tablet. Debossed "174" on one side and scored on the other.

📄 Package Label / Principal Display Panel 74 words ▾

PRINCIPAL DISPLAY PANEL - 90 Tablet Bottle Label 0.5 mg* FLUORIDE TABLETS BonGeo ™ PHARMACEUTICALS 52796-174-90 Floriva ™ 0.5 mg TABLETS Chewable Fluoride Multivitamin Quatrefolic ® Patent Ref.: U.S. Patent No. 7,947,662; Other patents pending Natural Berry Flavor Rx Dietary Supplement 90 Chewable Tablets *contains 0.5 mg fluoride from 1.1 mg sodium fluoride • SUGAR FREE AND GLUTEN FREE • NO ARTIFICIAL COLORS OR DYES • PRINCIPAL DISPLAY PANEL - 90 Tablet Bottle Label

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

Finished prescription product Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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 Drug Other". 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 BonGeo Pharmaceuticals, Inc.. 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 1 other package presentation of this same product, including 90 tablets (52796-0174-90). 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?
BonGeo Pharmaceuticals, 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 a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
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.
← 52796-0173-12 · BonGeo 52796-0177-90 · BonGeo →
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.