NDC 52796-0177-90 — Floriva VITAMIN A ACETATE, .BETA.-CAROTENE

🆔 Identity & classification

FDA NDC (as labeled) 52796-177-90

Product NDC 52796-177

11-digit billing NDC 52796017790

NCPDP billing unit EA — each (per item)

UNII 3LE3D9D6OY, 01YAE03M7J, PQ6CK8PD0R, 1C6V77QF41, H4N855PNZ1, X66NSO3N35 +10 more

UPC 0352796177900

SPL Set ID 768502e2-541f-4de8-ac68-3ab47c1f436d

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

GPI-14 78460000000520

GPI class Floriva

GCN Seq No 073064

GCN 37387

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 1 MG CHEWABLE TABLET

FDB brand name Floriva

Legend status Q — Non-drug — dietary supplement, vitamin, medical food, or herbal preparation

Why two NDCs? The FDA registers this code as 52796-177-90 — 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 → 52796-0177-90. 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

LabelerBonGeo Pharmaceuticals, Inc.

Labeler code52796

First marketedOct 2014

Product typeHuman Prescription Drug

Portfolio4 products on file

🔎 All NDCs from BonGeo Pharmaceuticals, Inc.

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

Label name FLORIVA 1 MG CHEWABLE TABLET Ingredient Pedi Multivit No.85/Fluoride

🧪 What is this product?

Floriva is a chewable tablet containing multiple vitamins and minerals. Vitamin A, beta-carotene, vitamin C, vitamin D, and vitamin E are typically included in products meant to support general nutrition and antioxidant function. The B vitamins (thiamine, riboflavin, niacinamide, pyridoxine, folic acid, and cyanocobalamin) are commonly found in formulations designed to support energy metabolism and nervous system function. Zinc and copper are trace minerals often included in nutritional supplements, while sodium fluoride is typically used in products intended to support dental health. This product is marketed without an approved FDA application.

Patient education

📘 MedlinePlus patient leaflet ↗

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.

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 system	Per each	Per 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price 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 ug 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 ugthis 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.

🔬 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 Floriva (this brand).

Top reported reactions

Drug Hypersensitivity2

Hospitalisation2

Surgery2

Acute Respiratory Failure1

Arthralgia1

Bacterial Infection1

Blood Pressure Increased1

Age at onset

Infant1

Reporter sex

Serious outcomes

Life-threatening1

Death1

Reports over time (by year) — tap or hover for the count & year

Most recent year is provisional (FAERS lags ~3 months).

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 NDC	Description	Marketing start	Status
52796-0177-90 You're viewing this	90 TABLET, CHEWABLE in 1 BOTTLE (52796-177-90)	2014-10-15	Active

🧭 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)	— Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 FDA registers it as 52796-177-90, 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: 52796-0177-90, written without dashes as 52796017790. 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 52796-0177-90, the first segment (52796) is the labeler code FDA assigned to BonGeo Pharmaceuticals, Inc.; the middle segment (0177) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (90) 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 BonGeo Pharmaceuticals, Inc.. Listing status can change — the directory data on this page refreshes weekly.

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.

📄 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

⏱️ 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 "177" on one side and scored on the other.

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

🔗 Related NDC lookups

🧪 All 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 NDCsSame ingredient 🏭 All BonGeo labeler NDCsLabeler code 52796 📚 All Copper Absorption Inhibitor NDCsDrug class

💊 Related drugs in this class

Other drugs that share this product’s specific therapeutic class — Pediatric Vitamin Preparations.

Multivit Infusion,Pedi 1,Vit K 54643-5646-01 Pedi Multivit No.17 W-Fluoride 58657-0163-01 Ped Mvit A,C,D3 No.21/Fluoride 58657-0323-50 Fat Emuls/Vit A/Vit D2/E/Vit K 65219-0337-62

Where does this data come from?

Other drugs sharing this product’s First Databank therapeutic class (HIC3). Each links to that NDC’s page in our directory.