Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Dr. Fibra Psyllium Husk 3.4 g Powder, 10 packets — NDC 55758-418-10 (Billing 55758-0418-10)
by Pharmadel LLC · 10 PACKET in 1 BOX / 1 POWDER in 1 PACKET
This is a package of 10 packets of Dr. Fibra Psyllium Husk 3.4 g Powder from Pharmadel LLC, marketed since Jun 2024 and currently FDA-listed. It is this product's only package size.
NDC 55758-0418-10
🏷️ FDA NDC (as labeled)
55758-418-10
billing pads the product segment with a zero
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
NDC database record
One package, one record: these facts belong to NDC 55758-418-10 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 55758 labeler · 418 product · 10 package
- Package marketed since
- Jun 30, 2024
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 5575841810 3
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
55758-418-10
Product NDC
55758-418
11-digit billing NDC
55758041810
RxCUI
824586
UNII
0SHO53407G
Application #
M007
SPL Set ID
1a6151c9-e1c4-f0c1-e063-6394a90aad24
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2024-06-30
Route
ORAL
Dosage form
POWDER
Substance
PSYLLIUM HUSK
Quick answers
- RxCUI (RxNorm): 824586
Why two NDCs?
The FDA registers this code as 55758-418-10 — 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 → 55758-0418-10. 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
Clinical
📗 Our plain-language guide HelloPharmacist
- Psyllium is used to relieve occasional constipation — meaning when you're having trouble going to the bathroom but it's not a long-term or ongoing problem. It comes in powder and c...
- These products are labeled for occasional constipation, and most can be taken up to 3 times a day. If you still haven't had relief after 7 days of use, that's your signal to stop a...
- This is really important — psyllium absorbs liquid and swells up to work as a fiber laxative. If you don't take it with a full 8-ounce glass of liquid, it can swell in your throat...
- Why do I have to drink so much water with it?
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.
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
💬 Questions about Psyllium Husk?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 8, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 55758-0418-10 You're viewing this Main listing | 10 PACKET in 1 BOX / 1 POWDER in 1 PACKET | 2024-06-30 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| up and up fiber therapy Natural Fiber 3.4 g/12g 11673-0668-90 | Target | 1368 g | — | — | FDA listed | — |
| up and up fiber therapy 3.4 g/5.79g 11673-0669-72 | TARGET | 425 g | — | — | FDA listed | — |
| Topco Fiber Therapy Sugar Free 3.4 g/5.79g 36800-0558-80 | TOPCO | 1040 g | — | — | FDA listed | — |
| Metamucil Therapy for Regularity 3.4 g/12g 37000-0023-04 | The | 30 packets | — | — | FDA listed | — |
| Metamucil Therapy for regularity 3.4 g/5.8g 37000-0024-04 | The | 30 packets | — | — | FDA listed | — |
| meijer Natural Fiber 3.4 g/12g 41250-0414-11 | MEIJER | 1368 g | — | — | FDA listed | — |
| meijer Natural Fiber 3.4 g/12g 41250-0455-11 | MEIJER | 1368 g | — | — | FDA listed | — |
| meijer fiber therapy 3.4 g/5.79g 41250-0508-18 | MEIJER | 425 g | — | — | FDA listed | — |
| Meijer Natural Daily Fiber Sugar Free Berry Flavor 3.4 g/5.78g 41250-0524-11 | MEIJER | 660 g | — | — | FDA listed | — |
| meijer Natural Fiber 3.4 g/12g 41250-0914-11 | MEIJER | 1368 g | — | — | FDA listed | — |
| Publix Fiber Therapy Orange Smooth 3.4 g/12g 41415-0513-48 | PUBLIX | 575 g | — | — | FDA listed | — |
| Publix Fiber Therapy Sugar Free 3.4 g/5.8g 41415-0515-14 | PUBLIX | 660 g | — | — | FDA listed | — |
| CAREONE Orange Flavored 3.4 g/5.8g 41520-0515-14 | FOODHOLD | 660 g | — | — | FDA listed | — |
| Dr. Fibra 3.4 gthis 55758-0418-10 | Pharmadel | 10 packets | — | — | FDA listed | — |
| Best Choice Fiber Therapy original coarse 3.4 g/7g 63941-0511-48 | BEST | 368 g | — | — | FDA listed | — |
| Best Choice Fiber Therapy Orange Flavor 3.4 g/12g 63941-0513-30 | BEST | 368 g | — | — | FDA listed | — |
| Premier Value Fiber Therapy Original Coarse 3.4 g/7g 68016-0511-72 | PHARMACY | 538 g | — | — | FDA listed | — |
| Premier Value Fiber Therapy Orange Flavor 3.4 g/12g 68016-0513-72 | PHARMACY | 861 g | — | — | FDA listed | — |
| Premier Value Orange Flavor 3.4 g/5.8g 68016-0551-14 | PHARMACY | 660 g | — | — | FDA listed | — |
| Daily Fiber Sugar Free 3.4 g/5.79g 68163-0515-48 | Raritan | 283 g | — | — | FDA listed | — |
| Unflavored Organic Natural Fiber 3.4 g/7g 68163-0570-85 | Raritan | 595 g | — | — | FDA listed | — |
| Natural Orange Flavor Organic Natural Fiber 3.4 g/12g 68163-0571-72 | Raritan | 864 g | — | — | FDA listed | — |
| Ultra Organic Fiber Sugar Free 3.4 g/7g 68163-0575-42 | Raritan | 300 g | — | — | FDA listed | — |
| Lidl Orange Smooth Fiber Powder Naturally and Artificially Flavored 3.4 g/12g 71141-0145-32 | LIDL | 861 g | — | — | FDA listed | — |
| LIDL Orange Smooth Fiber Powder Sugar Free Naturally and Artificially Flavored 3.4 g/5.8g 71141-0146-32 | LIDL | 660 g | — | — | 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2024
On the market since
Jun 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.
- FDA Orange Book · refreshed Oct 3, 2026
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.
🧪 Avoiding an ingredient? See Psyllium inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.
💡 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 H77VEI93A8
A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
-
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 8MDF5V39QO
A white powder form of baking soda that acts as a buffer and pH regulator in medicines. It helps maintain the right acid-base balance and may aid tablet disintegration.
-
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.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesanhydrous citric acid, FD&C yellow #6, flavors, povidone k-30, sodium bicarbonate, sucralose
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.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
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
LabelerPharmadel LLC
FDA applicationM007 (OTC MONOGRAPH DRUG)
Labeler code55758
First marketedJun 2024
Product typeHuman Otc Drug
Portfolio67 products on file
More NDCs from Pharmadel LLC labeler code 55758
- SanaTos Severe Cold Relief Nighttime Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride 25 mg; 10 mg; 650 mg Granule, For Solution NDC 55758-385-06
- Tabcin Extra Strength Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl, 250 mg; 5 mg; 2 mg; 10 mg Capsule, Liquid Filled NDC 55758-407-12
- Kingskin Salicylic acid 17 g/100mL Liquid NDC 55758-409-15
- Sanatos Multi Symptom Daytime Acetaminophen, Dextromethorphan HBr 20 mg/30mL; 650 mg/30mL Liquid NDC 55758-415-06
- Sanatos Multi Symptoms Nighttime Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate 650 mg/30mL; 12.5 mg/30mL; 30 mg/30mL Liquid NDC 55758-416-06
- Milagroso Camphor 10 g/100g Ointment NDC 55758-417-02
- Rapidol Sal Inglesa Magnesium Sulfate Heptahydrate 1 g/g Crystal NDC 55758-419-03
- Rapidol Hydrocortisone 1 g/100g Cream NDC 55758-420-03
- Antigrip Cough and Cold Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr 2 mg; 10 mg; 325 mg Capsule, Gelatin Coated NDC 55758-432-08
- DoloDent Toothache For adults Acetaminophen, Caffeine 65 mg; 500 mg Tablet NDC 55758-435-24
- Rapidol 500 Extra Strength ACETAMINOPHEN 500 mg Tablet NDC 55758-439-01
- Rapidol Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate 5000 [USP'U]/g; 400 [USP'U]/g; 3.5 mg/g Ointment NDC 55758-440-03
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 openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
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
📄 Do Not Use
📄 Ask a Doctor Before Use If
📄 Ask a Doctor or Pharmacist Before Use If
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
🤰 If Pregnant or Breast-Feeding
📄 Keep Out of Reach of Children
📄 Other Information
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses For relief of occasional constipation (irregularity). This product generally produces bowel movement in 12 to 72 hours.
⏱️ Dosage and Administration ▾
Directions mix this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid. Taking this product without enough liquid may cause choking. See choking warning. adults and children 12 years of age and older 1 packet up to 3 times a day children 6 to under 12 years of age 1/2 packet up to 3 times a day children under 6 years of age consult a doctor First time users: Start with the 1 packet per day, gradually increase to 3 times a day, as necessary.
As your body adjust to increased fiber intake, you may experience changes in bowel habits and/or minor bloating.
⚠️ Warnings ▾
Warnings Choking: Taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain, vomiting, or difficulty in swallowing or breathing after taking this product, seek immediate medical attention.
Allergy Alert: This product may cause allergic reactions in people, sensitive to inhaled or ingested psyllium. Do not use if allergic to any ingredient in this product Ask a doctor before use if you have abdominal pain, nausea or vomiting noticed a sudden change in bowel habits that persists over a period of 2 weeks a sodium restricted diet Ask a doctor or pharmacist before use if you are taking any other drug. Laxatives may affect how other drugs work.
When using this product take this product 2 hours before or after other drugs Stop use and ask a doctor if • constipation lasts more than 7 days • rectal bleeding occurs • you fail to have a bowel movement after use of a laxative. These may be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient and Purpose Active ingredient (in each packet) Purpose Psyllium seed husk 3.4 g.................... Bulk-forming laxative
🧪 Inactive Ingredients ▾
Inactive ingredients anhydrous citric acid, FD&C yellow #6, flavors, povidone k-30, sodium bicarbonate, sucralose
🎯 Purpose ▾
Active ingredient (in each packet) Purpose Psyllium seed husk 3.4 g.................... Bulk-forming laxative
📄 Do Not Use ▾
Do not use if allergic to any ingredient in this product
📄 Ask a Doctor Before Use If ▾
Ask a doctor before use if you have abdominal pain, nausea or vomiting noticed a sudden change in bowel habits that persists over a period of 2 weeks a sodium restricted diet
📄 Ask a Doctor or Pharmacist Before Use If ▾
Ask a doctor or pharmacist before use if you are taking any other drug. Laxatives may affect how other drugs work.
📄 When Using This Product ▾
When using this product take this product 2 hours before or after other drugs
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if • constipation lasts more than 7 days • rectal bleeding occurs • you fail to have a bowel movement after use of a laxative. These may be signs of a serious condition.
🤰 If Pregnant or Breast-Feeding ▾
If pregnant or breast-feeding, ask a health professional before use.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
📄 Other Information ▾
Other information each packet contains: potassium 36 mg; sodium 178 mg store below 86°F (30°C)
📄 Questions or Comments ▾
Questions? +1-866-359-3478 (M-F) 9 AM - 5 PM EST or www.pharmadel.com
📄 Package Label / Principal Display Panel ▾
Principal Display Panel Dr Fibra PDP BOX
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 ↗
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 Dr. Fibra (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 36%
Female · 64%
Unknown · 0%
Serious outcomes
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.
About this NDC listing & data coverage
Over-the-counter (OTC) product
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 "Otc Monograph Drug". 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 Pharmadel LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Pharmadel 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.
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.