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Vegetable Laxative SENNOSIDES, 8.6 mg 8.6 mg Tablet, Film Coated, 1,000-count — NDC 63561-0188-2 (Billing 63561-0188-02)

by Granulation Technology, Inc. · 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

This is a package of 1,000 tablets of Vegetable Laxative SENNOSIDES, 8.6 mg 8.6 mg Tablet, Film Coated from Granulation Technology, Inc., marketed since Jun 2025 and currently FDA-listed.

NDC 63561-0188-02
🏷️ FDA NDC (as labeled) 63561-0188-2 billing pads the package segment with a zero
This package
Contains1,000-count Pack sizes2 compare ↓
Product page 63561-0188-01 Also comes in: 100 tablets 63561-0188-1
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 →

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 63561-0188-2 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
63561 labeler · 0188 product · 2 package
Package marketed since
Jul 29, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6356101882 3
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 63561-0188-2
Product NDC 63561-0188
11-digit billing NDC 63561018802
RxCUI 312935
UNII 3FYP5M0IJX
Application # 505G(a)(3)
SPL Set ID 63dfe908-7cc0-41ca-9739-4b24ee14648e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-11
Route ORAL
Dosage form TABLET, FILM COATED
Substance SENNOSIDES
Quick answers
  • RxCUI (RxNorm): 312935
Why two NDCs? The FDA registers this code as 63561-0188-2 — a 5-4-1 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 package segment → 63561-0188-02. 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.

RxNorm drug class

This medicine belongs to the Contact laxatives class.

Drug family (ATC) Contact laxatives
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📗 Our plain-language guide HelloPharmacist
  • Senna typically produces a bowel movement within 6 to 12 hours. That's why most people take it at bedtime — so it can do its job overnight and you get results in the morning. If no...
  • How long does it take for senna to work?
  • Senna is designed for short-term, occasional use. You should not use it for more than 1 week unless your doctor specifically tells you it's okay. Using laxatives too often or for t...
  • Laxatives like senna can affect how your body absorbs other medications. To be safe, take senna at least 2 hours before or after any other drugs you use. It's always a good idea to...
📖 Read our full Senna guide →

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: 100 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
63561-0188-01 63561-0188-1 Main listing 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2025-06-11 — Active
63561-0188-02 You're viewing this 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2025-07-29 — Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 1,000-count package — 1000 tablet, film coated in 1 bottle, plastic.
How does this package differ from NDC 63561-0188-01?
Both are Vegetable Laxative SENNOSIDES, 8.6 mg 8.6 mg Tablet, Film Coated — the drug itself is identical. This page's package is the 1,000-count one, while NDC 63561-0188-01 is the 100 tablets package.
What NDC number is used to bill for this package of Vegetable Laxative SENNOSIDES, 8.6 mg 8.6 mg Tablet, Film Coated?
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
Vegetable Laxative 8.6 mg 63868-0579-01 CHAIN 100 tablets $0.021 — FDA listed —
Senna Laxative 8.6 mg 70677-0164-01 Strategic 100 tablets $0.024 — FDA listed —
Senna Laxative 8.6 mg 70677-1247-01 Strategic 150 tablets $0.026 — Availability likely —
Sennosides 8.6 mg 00904-7252-60 Major 100 tablets $0.026 — Availability likely —
Senna 8.6 mg 46122-0702-78 AmerisourceBergen 100 tablets $0.026 — Availability likely —
Sennosides 8.6 mg 70000-0610-01 LEADER/ 50 tablets $0.026 — Availability likely —
Senna Laxative 8.6 mg 70677-1097-01 Strategic 100 tablets $0.026 — Availability likely —
Senna 8.6 mg 82568-0006-01 AARNA 100 tablets $0.026 — Availability likely —
Senna 8.6 mg 83324-0004-01 QUALITY 100 tablets $0.026 — Availability likely —
Senokot 8.6 mg 67618-0300-10 Atlantis 100 tablets $0.247 — Availability likely —
Senna laxative 8.6 mg 00363-0138-10 Walgreens 100 tablets — — FDA listed —
Senna 8.6 mg 00363-8820-10 Walgreens 100 tablets — — FDA listed —
Senna Time 8.6 mg 00615-8402-39 NCS 30 tablets — — FDA listed —
Natural Senna Laxative 8.6 mg 00761-0790-02 Basic 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 00761-0798-02 Basic 100 tablets — — FDA listed —
Sennosides 8.6 mg 10135-0314-01 Marlex 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 11673-0191-01 TARGET 100 tablets — — FDA listed —
Senna 8.6 mg 11822-0298-02 Rite 100 tablets — — FDA listed —
Senna Tabs 8.6 mg 16103-0363-08 Pharbest 100 tablets — — FDA listed —
Vegetable Laxative 8.6 mg 21130-0998-01 BETTER 100 tablets — — FDA listed —
Kroger Senna Laxative Regular Strength 8.6 mg 30142-0710-00 KROGER 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 30142-0752-10 The 100 tablets — — FDA listed —
Laxative Senna 8.6 mg 36800-0984-01 TOPCO 100 tablets — — FDA listed —
Senna 8.6 mg 37808-0675-10 H 100 tablets — — FDA listed —
Senna 8.6 mg 37808-0782-10 H 100 tablets — — FDA listed —
Natural Laxative 8.6 mg 37835-0211-01 Bi-Mart 100 tablets — — FDA listed —
Senna laxative 8.6 mg 41163-0631-10 United 100 tablets — — FDA listed —
Senna laxative 8.6 mg 41163-0775-10 United 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 41163-0782-10 United 100 tablets — — FDA listed —
Meijer Senna Laxative Regular Strength 8.6 mg 41250-0445-00 MEIJER, 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 43063-0838-10 PD-Rx 10 tablets — — FDA listed —
Senna Time 8.6 mg 49483-0080-00 TIME 100000 tablets — — FDA listed —
Senna Laxative 8.6 mg 50804-0372-01 Good 100 tablets — — FDA listed —
Senna laxative 8.6 mg 50804-0882-10 Good 100 tablets — — Discontinued —
Sennosides 8.6 mg 51316-0112-02 CVS 250 tablets — — FDA listed —
CAREALL Sennosides 8.6 mg 51824-0058-01 New 100 tablets — — FDA listed —
Senna-Lax 8.6 mg 53041-0159-14 Guardian 50 tablets — — FDA listed —
Senna Natural Vegetable 8.6 mg 53329-0986-30 Medline 100 tablets — — FDA listed —
Sennosides Natural Laxative 8.6 mg 54257-0679-02 Magno-Humphries, 100 tablets — — FDA listed —
Sennosides 8.6 mg 55154-2347-00 Cardinal 1 tablet — — FDA listed —
Exchange select 8.6 mg 55301-0107-00 ARMY 100 tablets — — FDA listed —
Senna 8.6 mg 55319-0298-12 Family 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 55910-0208-12 DOLGENCORP, 100 tablets — — FDA listed —
Senna laxative 8.6 mg 55910-0882-10 Dolgencorp, 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 55910-0885-10 Dolgencorp, 100 tablets — — FDA listed —
Geri-kot 8.6 mg 57896-0434-01 Geri-Care 100 tablets — — FDA listed —
Geri-kot 8.6 mg 57896-0454-01 Geri-Care 100 tablets — — Discontinued —
Sennosides 8.6 mg 62993-0001-01 Morepen 30 tablets — — FDA listed —
Vegetable Laxative 8.6 mgthis 63561-0188-02 Granulation 1000 tablets — — FDA listed —
Senna laxative 8.6 mg 63941-0882-10 Best 100 tablets — — FDA listed —
Senna-Lax 8.6 mg 68998-0373-01 Marc 100 tablets — — FDA listed —
Senna Lax 8.6 mg 69168-0371-17 Allegiant 300 tablets — — FDA listed —
Senna 8.6 mg 69618-0064-01 Reliable 100 tablets — — FDA listed —
Sennosides 8.6 mg 69842-0220-08 CVS 500 tablets — — FDA listed —
Geri-kot 8.6 mg 71335-1806-01 Bryant 100 tablets — — FDA listed —
Senna 8.6 mg 71335-2360-01 Bryant 100 tablets — — FDA listed —
Sennosides 8.6 mg 71335-2660-01 Bryant 100 tablets — — FDA listed —
Senna 8.6 mg 71399-1017-01 Akron 100 tablets — — FDA listed —
Senna Natural Relief 8.6 mg 72090-0031-60 Pioneer 600 tablets — — FDA listed —
Senna Laxative 8.6 mg 72090-0041-01 Pioneer 300 tablets — — FDA listed —
Senna Laxative 8.6 mg 72476-0875-10 Care 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 72476-0882-10 Care 100 tablets — — FDA listed —
Sennosides 8.6 mg 72789-0283-10 PD-Rx 10 tablets — — FDA listed —
Senna-Tabs 8.6 mg 73057-0363-08 Ulai 100 tablets — — FDA listed —
Senna Lax 8.6 mg 76162-0005-98 TopCo 200 tablets — — FDA listed —
Vegetable Laxative 8.6 mg 79903-0064-10 Wal-Mart 100 tablets — — FDA listed —
Vegetable Laxative 8.6 mg 79903-0322-10 Walmart 100 tablets — — FDA listed —
Senna Laxative 8.6 mg 80136-0434-01 Heartland 100 tablets — — FDA listed —
Senna 8.6 mg 82804-0143-04 Proficient 4 tablets — — FDA listed —
Senna Laxative 8.6 mg 84324-0012-01 NUVICARE 200 tablets — — FDA listed —
Dr Simi Regular Strength Sennosides 8.6mg 8.6 mg 85786-0501-50 Farmacias 50 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

🏛️
2025
On the market since
Jun 2025
📍
2026
Currently FDA-listed
1 year 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 brown
ShapeRound
ImprintG188
Size1 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 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 M28OL1HH48
    Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
  • UNII O7TSZ97GEP
    A mineral compound that serves as a filler and binding agent in tablets and capsules. It adds bulk to the medicine and helps hold ingredients together during manufacturing.
  • 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 4R4HFI6D95
    Polyethylene glycol 4000 is a synthetic polymer derived from petroleum. It serves as a binder, filler, and lubricant in solid dosage forms, and helps control how quickly the medicine dissolves.
  • UNII 532B59J990
    Polyvinyl alcohol is a synthetic polymer made from plant-derived materials. It's used as a binder to hold ingredients together, a film-former in coatings, and a thickener in liquid formulations.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • 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.
  • 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.

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

The official label also statescroscarmellose sodium,dibasic calcium phosphate dihydrate, microcrystalline cellulose, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, polyvinyl alcohol, polyethylene glycol (PEG) 4000, talc

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.

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

LabelerGranulation Technology, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code63561
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from Granulation Technology, Inc. labeler code 63561

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.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 How Supplied / Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 2 words ▾

Drug Facts

⏱️ Dosage and Administration 77 words ▾

Directions Take preferably at bedtime or as directed by a doctor age starting dosage maximum dosage adults and children 12 years of age and over 2 tablets once a day 4 tablets twice a day children 6 to under 12 years 1 tablet once a day 2 tablets twice a day children 2 to under 6 years 1/2 tablet once a day 1 tablet twice a day children under 2 years ask a doctor ask a doctor

⚠️ Warnings 1 words ▾

Warnings

📦 How Supplied / Storage and Handling 12 words ▾

Other information Each tablet contains: Calcium 27.93 mg Store between 20-25°C (68-77°F)

🧪 Active Ingredient 8 words ▾

Active ingredients (in each tablet) Sennosides 8.6 mg

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients croscarmellose sodium,dibasic calcium phosphate dihydrate, microcrystalline cellulose, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, polyvinyl alcohol, polyethylene glycol (PEG) 4000, talc

🎯 Purpose 2 words ▾

Purpose Laxative

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
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 — Not published for this NDC No photo available yet for this listing.
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 Granulation Technology, 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 100 tablets (63561-0188-01). 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?
Granulation Technology, 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 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.
← 63561-0187-01 · Granulation 63561-0197-01 · Granulation →
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.