H E B Stool Softener laxative DOCUSATE SODIUM 250 mg Capsule, Liquid Filled, 140-count
by H E B · 140 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-293-88)
NDC 37808-0293-88
🏷️ FDA NDC (as labeled)
37808-293-88
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 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)
37808-293-88
Product NDC
37808-293
11-digit billing NDC
37808029388
RxCUI
1245468
UNII
F05Q2T2JA0
UPC
0041220280391
Application #
M007
SPL Set ID
9d848fdd-3a2f-45c6-9ff3-17f1d74e0f4f
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2021-10-14
Route
ORAL
Dosage form
CAPSULE, LIQUID FILLED
Substance
DOCUSATE SODIUM
Why two NDCs?
The FDA registers this code as 37808-293-88 — 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 → 37808-0293-88. 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 Softeners, emollients class.
Drug family (ATC)
Softeners, emollients
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.
🏭 Manufacturer & labeler
LabelerH E B
FDA applicationM007 (OTC MONOGRAPH DRUG)
Labeler code37808
First marketedOct 2021
Product typeHuman Otc Drug
Portfolio264 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?
This is an over-the-counter liquid-filled capsule containing docusate sodium, a stool softener. Taken by mouth, docusate sodium is typically used to soften stool and make bowel movements easier, especially for people who want to avoid straining. This product is marketed under the FDA's OTC monograph rules for laxatives and stool softeners, rather than as an individually reviewed drug application.
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Docusate Sodium — tap one for details:
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 DOCUSATE SODIUM?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
red / white
ShapeCapsule
ImprintSCU1
Size2 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.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.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 mL | 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 |
|---|---|---|---|---|---|---|
| Stool Softener Laxative 250 mg 00904-7281-60 | Major | 100 capsules | $0.052 | — | Availability likely | — |
| Good Neighbor Stool Softener laxative 250 mg 46122-0693-78 | AmerisourceBergen | 100 capsules | $0.052 | — | Availability likely | — |
| Stool Softener 250 mg 46122-0826-74 | Amerisource | 100 capsules | $0.052 | — | Availability likely | — |
| Docusate Sodium 250 mg 50268-0268-15 | AvPAK | 1 capsule | $0.052 | — | Availability likely | — |
| Stool Softener 250 mg 70677-1096-01 | Strategic | 100 capsules | $0.052 | — | Availability likely | — |
| Preferred Stool Softener laxative 250 mg 10956-0781-00 | Reese | 140 capsules | — | — | FDA listed | — |
| Stool Softener Laxative 250 mg 17856-7281-01 | ATLANTIC | 1 capsule | — | — | FDA listed | — |
| Stool Softener Laxative Extra Strength 250 mg 36800-0568-10 | TOP | 100 capsules | — | — | Discontinued | — |
| Stool Softener 250 mg 36800-0640-10 | TOP | 100 capsules | — | — | FDA listed | — |
| H E B Stool Softener laxative 250 mgthis 37808-0293-88 | H | 140 capsules | — | — | FDA listed | — |
| Stool Softener 250 mg 37808-0585-14 | HEB | 140 capsules | — | — | FDA listed | — |
| Stool Softener 250 mg 37808-0879-14 | H | 140 capsules | — | — | FDA listed | — |
| Stool Softener 250 mg 37835-0223-01 | Bi-Mart | 100 capsules | — | — | FDA listed | — |
| Stool Softener Extra Strength 250 mg 41250-0859-10 | MEIJER, | 100 capsules | — | — | FDA listed | — |
| Stool Softener Extra Strength 250 mg 49035-0378-14 | EQUATE | 140 capsules | — | — | FDA listed | — |
| Prolaxa 250 mg 53225-2001-01 | Terrain | 100 capsules | — | — | FDA listed | — |
| Docusate Sodium 250 mg 53345-0035-01 | Humanwell | 7000 capsules | — | — | FDA listed | — |
| Docusate Sodium 250 mg 54629-0601-01 | National | 100 capsules | — | — | FDA listed | — |
| Docusate Sodium 250 mg 55154-4341-00 | Cardinal | 1 capsule | — | — | Discontinued | — |
| Stool Softener Extra Strength 250 mg 55910-0879-10 | Dolgencorp, | 100 capsules | — | — | FDA listed | — |
| Stool Softener 250 mg 57896-0426-01 | Geri-Care | 100 capsules | — | — | FDA listed | — |
| Stool Softener Extra Strength 250 mg 59726-0058-25 | P | 250 capsules | — | — | FDA listed | — |
| Stool Softener Laxative Extra Strength 250 mg 59726-0059-10 | P | 100 capsules | — | — | FDA listed | — |
| Stool Softener Laxative Extra Strength 250 mg 59726-0879-10 | P | 100 capsules | — | — | FDA listed | — |
| Quality Choice Stool Softener laxative 250 mg 63868-0662-01 | Chain | 100 capsules | — | — | FDA listed | — |
| Colace Extra Strength Stool Softner 250 mg 67618-0201-12 | Atlantis | 60 capsules | — | — | FDA listed | — |
| Stool Softener Laxative 250 mg 68016-0471-01 | Chain | 100 capsules | — | — | FDA listed | — |
| Stool Softener Extra Strength 250 mg 68016-0587-00 | Chain | 100 capsules | — | — | FDA listed | — |
| Stool Softener 250 mg 68071-5297-06 | NuCare | 60 capsules | — | — | FDA listed | — |
| Stool Softener Extra Strength 250 mg 69842-0740-25 | CVS | 250 capsules | — | — | FDA listed | — |
| Stool Softener Extra Strength 250 mg 69842-0879-25 | CVS | 250 capsules | — | — | FDA listed | — |
| Stool Softener 250 mg 71335-1677-01 | Bryant | 30 capsules | — | — | FDA listed | — |
| Docusate Sodium 250 mg 72789-0166-60 | PD-Rx | 60 capsules | — | — | FDA listed | — |
| Topcare Stool Softener laxative 250 mg 76162-0764-10 | TOPCO | 100 capsules | — | — | FDA listed | — |
| Stool Softener Laxative Extra Strength 250 mg 79903-0073-14 | WALMART | 140 capsules | — | — | FDA listed | — |
| Prolaxa 250 mg 80425-0540-01 | Advanced | 100 capsules | — | — | FDA listed | — |
| Docusate Sodium, Extra Strength 250 Mg 80513-0100-01 | Advanced | 100 capsules | — | — | FDA listed | — |
| Docusate Sodium, Extra Strength 250 Mg 80513-0101-01 | Advanced | 100 capsules | — | — | FDA listed | — |
| Stool Softener Laxative 250 mg 71335-2313-01 | Bryant | 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
🏛️
2021
On the market since
Oct 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.
🔬 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 H E B Stool Softener laxative (this brand).
Top reported reactions
Reporter sex
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 37808-0293-88 You're viewing this | 140 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-293-88) | 2021-10-14 | Active |
🧭 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) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 FDA registers it as 37808-293-88, 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: 37808-0293-88, written without dashes as 37808029388. 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 37808-0293-88, the first segment (37808) is the labeler code FDA assigned to H E B; the middle segment (0293) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (88) 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 H E B. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
H E B 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.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses relieves occasional constipation (irregularity) generally produces a bowel movement in 12 to 72 hours
⏱️ Dosage and Administration ▾
Directions Take only by mouth. Doses may be taken as a single daily dose or in divided doses. adults and children 12 years and over take 1 to 3 softgels daily children 2 to under 12 years of age take 1 softgel daily children under 2 years ask a doctor
⚠️ Warnings ▾
Warnings Do not use if you are presently taking mineral oil, unless told to do so by a doctor Ask a doctor before use if you have stomach pain nausea vomiting noticed a sudden change in bowel movements that lasts over 2 weeks Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition. you need to use a stool softener laxative for more than 1 week 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.
📦 Storage and Handling ▾
Other information each softgel contains: sodium 7 mg store at room temperature 15° to 30°C (59° to 86°F) Image of carton
🧪 Active Ingredient ▾
Active ingredient (in each softgel) Docusate Sodium 250 mg
🧪 Inactive Ingredients ▾
Inactive Ingredients FD&C RED #40, FD&C YELLOW #6, GELATIN, GLYCEROL, POLYETHYLENE GLYCOL, PURIFIED WATER, SORBITOL.
🎯 Purpose ▾
Purpose Stool softener
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.