JBA Collagen-Electrolyte Mocktail Vitamin C,Thiamin,Riboflavin,Niacin,Vitamin B6,Folate,Biotin,Pantothenic Acid,Magnesium,Zinc,Sodium,Potassium,Bovine Collagen Peptides 100 mg/12g; 1.2 mg/12g; 1.6 mg/12g; 18 mg/12g; 2.5 mg/12g; 200 ug/12g; 80 ug/12g; 6 mg/12g; 50 mg/12g; 10 mg/12g; 250 mg/12g; 190 mg/12g Powder
by Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals · 5 PACKET in 1 BOX (13411-848-05) / 12 g in 1 PACKET
NDC 13411-0848-05
🏷️ FDA NDC (as labeled)
13411-848-05
billing pads the product segment with a zero
This package
Contains12 g in 1 packet
Pack sizes3 compare ↓
OTC
On market
Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
13411-848-05
Product NDC
13411-848
11-digit billing NDC
13411084805
UNII
PQ6CK8PD0R, X66NSO3N35, TLM2976OFR, 2679MF687A, KV2JZ1BI6Z, 935E97BOY8 +6 more
SPL Set ID
e0199be5-0c51-411a-a184-225c1e6e602f
Established class (EPC)
Vitamin C; Nicotinic Acid; Vitamin B6 Analog
Chemical class
Ascorbic Acid; Nicotinic Acids; Vitamin B 6; Analogs/Derivatives
DEA schedule
Non-controlled
Marketing category
UNAPPROVED DRUG OTHER
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2024-03-22
Route
ORAL
Dosage form
POWDER
Substance
ASCORBIC ACID; THIAMINE; RIBOFLAVIN; NIACIN; PYRIDOXINE; FOLIC ACID; BIOTIN; PANTOTHENIC ACID; MAGNESIUM; ZINC; SODIUM; POTASSIUM
Why two NDCs?
The FDA registers this code as 13411-848-05 — 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 → 13411-0848-05. 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
LabelerAdvanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Labeler code13411
First marketedMar 2024
Product typeHuman Otc Drug
Portfolio16 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?
JBA Collagen-Electrolyte Mocktail is an oral powder containing a mix of B vitamins, vitamin C, minerals, and bovine collagen peptides. The B vitamins (thiamine, riboflavin, niacin, vitamin B6, folate, biotin, and pantothenic acid) and vitamin C are typically found in nutritional supplements and are commonly used to support energy metabolism and general wellness. The minerals magnesium, zinc, sodium, and potassium function as electrolytes, which are commonly included in hydration and recovery products. Bovine collagen peptides are a protein source often used in nutritional formulations. This product is marketed as an unapproved drug and has not received FDA approval.
Patient education
Supplement & herbal interactions
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.
💬 Questions about Vitamin C,Thiamin,Riboflavin,Niacin,Vitamin B6,Folate,Biotin,Pantothenic Acid,Magnesium,Zinc,Sodium,Potassium,Bovine Collagen Peptides?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 XF417D3PSL
Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
-
UNII 7CVR7L4A2D
A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
-
UNII 3OWL53L36A
A natural sugar alcohol derived from seaweed or synthesized in the lab. It's used as a filler to add bulk, a sweetener in sugar-free formulas, and a disintegrant to help tablets break apart in the stomach.
-
UNII U725QWY32X
Povidone K30 is a synthetic polymer made from petroleum. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in the stomach so the medicine can be absorbed.
-
UNII 6TC6NN0876
A natural sweetener extracted from stevia plant leaves. It sweetens the medicine to improve taste without adding calories, helping make medications easier to take.
-
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.
6 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.
💲 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 g | 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 |
|---|---|---|---|---|---|---|
| JBA Collagen-Electrolyte Mocktail 100 mg/12g; 1.2 mg/12g; 1.6 mg/12g; 18 mg/12g; 2.5 mg/12g; 200 ug/12g; 80 ug/12g; 6 mg/12g; 50 mg/12g; 10 mg/12g; 250 mg/12g; 190 mg/12gthis 13411-0848-05 | Advanced | 5 packets | — | — | 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
Mar 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 13411-0848-05 You're viewing this | 5 PACKET in 1 BOX (13411-848-05) / 12 g in 1 PACKET | 2024-03-22 | Active |
| 13411-0848-15 | 15 PACKET in 1 BOX (13411-848-15) / 12 g in 1 PACKET | 2024-03-22 | Active |
| 13411-0848-30 | 30 PACKET in 1 BOX (13411-848-30) / 12 g in 1 PACKET | 2024-03-22 | Active |
Pack size FAQ
What quantity is in NDC 13411-0848-05?
NDC 13411-0848-05 is listed by the FDA — 5 packet in 1 box / 12 g in 1 packet.
What NDC number is used to bill for this package of JBA Collagen-Electrolyte Mocktail Vitamin C,Thiamin,Riboflavin,Niacin,Vitamin B6,Folate,Biotin,Pantothenic Acid,Magnesium,Zinc,Sodium,Potassium,Bovine Collagen Peptides 100 mg/12g; 1.2 mg/12g; 1.6 mg/12g; 18 mg/12g; 2.5 mg/12g; 200 ug/12g; 80 ug/12g; 6 mg/12g; 50 mg/12g; 10 mg/12g; 250 mg/12g; 190 mg/12g Powder?
Bill NDC 13411-0848-05 — the 11-digit billing format is 13411084805. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 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 FDA registers it as 13411-848-05, 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: 13411-0848-05, written without dashes as 13411084805. 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 13411-0848-05, the first segment (13411) is the labeler code FDA assigned to Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals; the middle segment (0848) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (05) 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 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 packets (13411-0848-15), 30 packets (13411-0848-30). 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.
📄 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 ▾
Direction Your morning self-care ritual: Pour one packet into your favorite glass Add 8-12 oz water to taste Drink promptly and enjoy!
⚠️ Warnings ▾
Warnings BEFORE USING this dietary supplement ask your doctor if you Are considering using this product as part of a cholesterol lowering program Are using medication to control your blood sugar levels Have recently experienced abdominal pain, nausea, vomiting or a sudden change in bowel habits persisting for two weeks. Warning : Bulk forming fibers like psyllium husk may affect how well medicines work. Take this product at least 2 hours before or after medicines.
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.