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JBA Joint Revive Glucosamine Sulfate Potassium Chloride,White Willow Bark Extract,Eggshell Membrane Collagen,Chondroitin Sulfate,Turmeric Root Extract,Bromelain,Soy Lecithin 160 mg; 300 mg; 150 mg; 100 mg; 50 mg; 10 mg; 5 mg Capsule, 30-count — NDC 13411-0856-30 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

JBA Joint Revive Glucosamine Sulfate Potassium Chloride,White Willow Bark Extract,Eggshell Membrane Collagen,Chondroitin Sulfate,Turmeric Root Extract,Bromelain,Soy Lecithin 160 mg; 300 mg; 150 mg; 100 mg; 50 mg; 10 mg; 5 mg Capsule, 30-count — NDC 13411-856-30 (Billing 13411-0856-30)

by Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals · 30 CAPSULE in 1 BOTTLE

This is a package of 30 capsules of JBA Joint Revive Glucosamine Sulfate Potassium Chloride,White Willow Bark Extract,Eggshell Membrane Collagen,Chondroitin Sulfate,Turmeric Root Extract,Bromelain,Soy Lecithin 160 mg; 300 mg; 150 mg; 100 mg; 50 mg; 10 mg; 5 mg Capsule from Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals, marketed since Aug 2024 and currently FDA-listed.

NDC 13411-0856-30
🏷️ FDA NDC (as labeled) 13411-856-30 billing pads the product segment with a zero
This package
Contains30-count Pack sizes3 compare ↓
Product page 13411-0856-15 Also comes in: 15 capsules 13411-856-15 60 capsules 13411-856-60
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Aug 27, 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 13411-856-30 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
13411 labeler · 856 product · 30 package
Package marketed since
Aug 13, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 1341185630 3
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 13411-856-30
Product NDC 13411-856
11-digit billing NDC 13411085630
UNII 205MXS71H7, 15VQ11I66N, N7QBR4212V, 6IC1M3OG5Z, 856YO1Z64F, ZLM4P8929R +1 more
SPL Set ID 27f5acf3-04f6-49d7-bbf5-f1c3ad6200cc
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-08-13
Route ORAL
Dosage form CAPSULE
Substance SALIX ALBA BARK; GLUCOSAMINE SULFATE POTASSIUM CHLORIDE; EGG SHELL MEMBRANE; CHONDROITIN SULFATE (BOVINE); TURMERIC; STEM BROMELAIN; SOYBEAN LECITHIN
Why two NDCs? The FDA registers this code as 13411-856-30 — 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 → 13411-0856-30. 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?

JBA Joint Revive is an oral capsule containing seven plant-derived and animal-derived ingredients. Glucosamine sulfate, chondroitin sulfate, and eggshell membrane collagen are components commonly included in products intended to support joint structure and function. White willow bark extract, turmeric root extract, and bromelain are plant compounds typically used in formulations designed to address joint comfort. Soy lecithin functions as an emulsifier. 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: 15 capsules 60 capsules
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
13411-0856-15 13411-856-15 Main listing 15 CAPSULE in 1 BOTTLE 2024-08-13 — Active
13411-0856-30 You're viewing this 30 CAPSULE in 1 BOTTLE 2024-08-13 — Active
13411-0856-60 13411-856-60 60 CAPSULE in 1 BOTTLE 2024-08-13 — Active

You're viewing one of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 30-count package — 30 capsule in 1 bottle.
How does this package differ from NDC 13411-0856-15?
Both are JBA Joint Revive Glucosamine Sulfate Potassium Chloride,White Willow Bark Extract,Eggshell Membrane Collagen,Chondroitin Sulfate,Turmeric Root Extract,Bromelain,Soy Lecithin 160 mg; 300 mg; 150 mg; 100 mg; 50 mg; 10 mg; 5 mg Capsule — the drug itself is identical. This page's package is the 30-count one, while NDC 13411-0856-15 is the 15 capsules package.
What NDC number is used to bill for this package of JBA Joint Revive Glucosamine Sulfate Potassium Chloride,White Willow Bark Extract,Eggshell Membrane Collagen,Chondroitin Sulfate,Turmeric Root Extract,Bromelain,Soy Lecithin 160 mg; 300 mg; 150 mg; 100 mg; 50 mg; 10 mg; 5 mg Capsule?
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
JBA Joint Revive 160 mg/1; 300 mg/1; 150 mg/1; 100 mg/1; 50 mg/1; 10 mg/1; 5 mgthis 13411-0856-30 Advanced 30 capsules — — 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
Aug 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.

What it looks like

Color yellow
ShapeCapsule
Size23 mm
ScoringNot scored
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 O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.

3 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

LabelerAdvanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Labeler code13411
First marketedAug 2024
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from Advanced Pharmaceutical Services, Inc. Dba Affor... labeler code 13411

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.
⏱️ Dosage and Administration ⚠️ Warnings ⚠️ Precautions 📄 Package Label / Principal Display Panel
⏱️ Dosage and Administration 9 words ▾

Direction Take 2-3 capsules daily, preferably with a meal.

⚠️ Warnings 8 words ▾

Other Ingredients Maize starch, Microcrystalline Cellulose, Magnesium Stearate.

⚠️ Precautions 47 words ▾

If you are pregnant, may become pregnant or are breast feeding, consult your healthcare professional before using this product. Do not use if tamper-evident seal is broken or missing. Keep Out of The Reach of Children. Store in a cool, dry place (59°F-86°F), avoid moisture and light.

📄 Package Label / Principal Display Panel 4 words ▾

Product label image description

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 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 Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals. 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 2 other package presentations of this same product, including 15 capsules (13411-0856-15), 60 capsules (13411-0856-60). 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?
Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals 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.
← 13411-0848-05 · Advanced 13411-0857-15 · Advanced →
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.