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Natural Senna Laxative Sennosides 8.6 mg Tablet, 100-count — NDC 00761-0790-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Natural Senna Laxative Sennosides 8.6 mg Tablet, 100-count — NDC 0761-0790-02 (Billing 00761-0790-02)

by Basic Drugs, Inc. · 100 TABLET in 1 BOTTLE

This is a package of 100 tablets of Natural Senna Laxative Sennosides 8.6 mg Tablet from Basic Drugs, Inc., marketed since Dec 2021 and currently FDA-listed. It is this product's only package size.

NDC 00761-0790-02
🏷️ FDA NDC (as labeled) 0761-0790-02 billing pads the labeler segment with a zero
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 0761-0790-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0761 labeler · 0790 product · 02 package
Package marketed since
Dec 14, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 0761079002 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0761-0790-02
Product NDC 0761-0790
11-digit billing NDC 00761079002
RxCUI 312935
UNII 3FYP5M0IJX
Application # 505G(a)(3)
SPL Set ID d32ab3e7-7942-7420-e053-2a95a90aa024
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-12-14
Route ORAL
Dosage form TABLET
Substance SENNOSIDES
Quick answers
  • RxCUI (RxNorm): 312935
Why two NDCs? The FDA registers this code as 0761-0790-02 — a 4-4-2 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 labeler segment → 00761-0790-02. 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

📖 What it is MedlinePlus · NLM

Senna is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Senna is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.

Read the full MedlinePlus article ↗
📗 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 →
3
Nutrient depletion considerations

Sennosides (OTC drug) may be associated with lower levels of 3 nutrients — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Sennosides (OTC drug) nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.
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
00761-0790-02 You're viewing this Main listing 100 TABLET in 1 BOTTLE 2021-12-15 — Active

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 mgthis 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 mg 63561-0188-01 Granulation 100 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 —
Laxative 8.6 mg 55910-0659-10 Dolgencorp, 100 tablets — — FDA listed —
Sennosides 8.6 mg 87717-0501-01 Morepen 1000 tablets — — FDA listed —
HyVee Regular Strength Sennosides Laxative 8.6 mg 42507-0155-01 HyVee 100 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

🏛️
2021
On the market since
Dec 2021
📍
2026
Currently FDA-listed
5 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 brown
ShapeRound
ImprintAZ217
Size8 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 L11K75P92J
    A mineral salt made from calcium and phosphate. It acts as a filler and binder in tablets to add bulk and help hold the medicine together in solid form.
  • 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 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 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.

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

The official label also statesCollodial silicon dioxide, croscarmellose sodium, dibasic calcium phosphate, magnesium stearate, microcrystalline cellulose.

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

LabelerBasic Drugs, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code00761
First marketedDec 2021
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from Basic Drugs, Inc. labeler code 00761

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 16 words ▾

Uses for the relief of occasional constipation generally causes bowel movement in 6 to 12 hours

⏱️ Dosage and Administration 116 words ▾

Directions take preferably at bedtime or as directed by a doctor If you do not have a confortable bowel movement by the second day, increase dosage by one tablet (do not exceed the maximum dosage) or decrease dose until you are confortable. adults and children 12 years and over take 2 tablets once a day. do not take more than 4 tablets twice a day. children 6 to under 12 years take 1 tablet once a day. do not take more than 2 tablets twice a day. children 2 to under 6 years take 1/2 tablet once a day. do not take more than 1 tablet twice a day. children under 2 years ask a doctor

⚠️ Warnings 127 words ▾

Warnings Do not use laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor. Ask a doctor before use if you have noticed a sudden change in bowel habits that persists over a period of 2 weeks. Ask a doctor or pharmacist before use if you are taking a prescription drug.

Laxatives may affect how other drugs work. Take this product 2 or more hours before or after other drugs. When using this product do not use for a period longer than 1 week.

Stop use and ask a doctor if rectal bleeding or failure to have a bowel movement occur after use of a laxative. These may indicate a serious condition. If pregnant or breast-feeding, ask a health professional before use.

🧪 Active Ingredient 7 words ▾

Active ingredient (in each tablet) SENNOSIDES 8.6MG

🧪 Inactive Ingredients 14 words ▾

Inactive ingredients Collodial silicon dioxide, croscarmellose sodium, dibasic calcium phosphate, magnesium stearate, microcrystalline cellulose.

🎯 Purpose 2 words ▾

Purpose LAXATIVE

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

📄 Other Information 11 words ▾

Other information each tablet contains: calcium 40mg store at room temperature

📄 Questions or Comments 2 words ▾

Questions? 937-898-4010

📄 Package Label / Principal Display Panel 1 words ▾

label

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 ✓ 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 Basic Drugs, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Basic Drugs, 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.
← 00713-5521-01 · Cosette 00761-0798-02 · Basic →
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.