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Walgreens Stool Softener Fruit Punch Docusate sodium 50 mg/5mL Liquid, 237 mL — NDC 00363-7140-08 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Walgreens Stool Softener Fruit Punch Docusate sodium 50 mg/5mL Liquid, 237 mL — NDC 0363-7140-08 (Billing 00363-7140-08)

by WALGREENS CO. · 237 mL in 1 BOTTLE, PLASTIC

This is a package of 237 mL of Walgreens Stool Softener Fruit Punch Docusate sodium 50 mg/5mL Liquid from WALGREENS CO., marketed since Apr 2019 and currently FDA-listed. It is this product's only package size.

NDC 00363-7140-08
🏷️ FDA NDC (as labeled) 0363-7140-08 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0363-7140-08
Product NDC 0363-7140
11-digit billing NDC 00363714008
RxCUI 1248119
UNII F05Q2T2JA0
Application # M007
SPL Set ID 8428c81d-227a-4b0f-9a47-71d6a6983842
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-04-25
Route ORAL
Dosage form LIQUID
Substance DOCUSATE SODIUM
Quick answers
  • RxCUI (RxNorm): 1248119
Why two NDCs? The FDA registers this code as 0363-7140-08 — 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 → 00363-7140-08. 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.

Clinical

🧪 What is this product?

This is an over-the-counter liquid stool softener taken by mouth, containing docusate sodium. Docusate sodium is commonly used to soften stool and ease bowel movements by increasing water content in the intestines. The product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for this category of product rather than undergoing individual approval.

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 mLPer 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
00363-7140-08 You're viewing this Main listing 237 mL in 1 BOTTLE, PLASTIC 2019-04-25 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Docusate Sodium Liquid 50 mg/5mL 00536-1304-85 RUGBY 473 ml $0.020 — Availability likely —
Docusate Sodium Liquid 50 mg/5mL 54859-0813-16 LLORENS 473 ml $0.020 — Availability likely —
Docusate Sodium 50 mg/5mL 00121-0935-16 PAI 473 ml $0.021 — Discontinued —
Walgreens Stool Softener Fruit Punch 50 mg/5mLthis 00363-7140-08 WALGREENS 237 ml — — FDA listed —
Kroger Stool Softener Fruit Punch 50 mg/5mL 41226-0714-08 KROGER 237 ml — — FDA listed —
Docusate Sodium 50 mg/5mL 48433-0220-10 Safecor 10 ml — — FDA listed —
GeriCare Docusate Sodium Liquid 50 mg/5mL 57896-0413-16 GERI-CARE 473 ml — — FDA listed —
GeriCare Docusate Sodium Liquid 50 mg/5mL 57896-0423-16 GERI-CARE 473 ml — — FDA listed —
CVS Stool Softener Fruit Punch 50 mg/5mL 69842-0714-08 CVS 237 ml — — FDA listed —
Docusate Sodium Oral Liquid 100 mg/10mL 81033-0022-50 Kesin 100 cups — — FDA listed —
Docusate Sodium 100 mg/10mL 84447-0011-01 Belleview 200000 ml — — FDA listed —
Docusate Sodium 50 mg/5mL 55154-2346-05 Cardinal 5 cups — — 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

🏛️
2019
On the market since
Apr 2019
📍
2026
Currently FDA-listed
7 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.

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.

Manufacturer & labeler

LabelerWALGREENS CO.
FDA applicationM007 (OTC MONOGRAPH DRUG)
Labeler code00363
First marketedApr 2019
Product typeHuman Otc Drug
Portfolio73 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.

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 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 14 words ▾

Uses relieves occasional constipation (irregularity) generally produces bowel movement in 12 to 72 hours

⏱️ Dosage and Administration 89 words ▾

Directions follow dosing directions below or take as directed by doctor must be given in a 6 to 8 oz glass of milk or fruit juice to prevent throat irritation may be taken as a single daily dose or in divided doses take maximum dose daily until first bowel movement, dosage should then be reduced according to individual response. do not exceed recommended dose shake well before using Age Dose Adults and children 12 years and over 5 mL-30 mL Children 2 to under 12 years 5 mL-15 mL

⚠️ Warnings 71 words ▾

Warnings Do not use laxative products for longer than 1 week unless directed by a doctor Ask a doctor before use if you have stomach pain nausea vomiting noticed a sudden change in bowel habits that continues over a period of 2 weeks Stop use and ask a doctor if you have rectal bleeding of fail to have a bowel movement after use of laxative. These may indicate a serious condition.

🧪 Active Ingredient 10 words ▾

Active ingredient (in each 5 mL) Docusate Sodium 50 mg

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients citric acid, flavor, potassium sorbate, polyethylene glycol, povidone, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum. Questions or comments? 1-866-467-2748

🎯 Purpose 3 words ▾

Purpose Stool Softener

🤰 If Pregnant or Breast-Feeding 12 words ▾

If pregnant or breast feeding , ask a health professional before use.

📄 Keep Out of Reach of Children 24 words ▾

Keep out of reach of children . In case of overdose, get medical help or contact a poison control Center right away at 1-800-222-1222.

📄 Other Information 40 words ▾

Other information each 5 mL contains: sodium 6 mg low sodium store at room temperature protect from excessive heat keep tightly closed protect from light SAFETY SEALED: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING

📄 Questions or Comments 4 words ▾

Questions or comments? 1-866-467-2748

📄 Package Label / Principal Display Panel 100 words ▾

Principal Display Panel NDC 0363-7140-08 Compare to Colace® Clear active ingredient †† Walgreens Stool Softener DOCUSATE SODIUM 50 MG/5 ML STOOL SOFTENER LIQUID Effective relief of occasional constipation FRUIT PUNCH FLAVOR NATURALLY AND ARTIFICIALLY FLAVOR 8 FL OZ (237 mL) Package Contains One Bottle DISTRIBUTED BY: WALGREEN CO. 200 WILMOT RD., DEERFIELD, IL 60015 Walgreens 100 % SATISFACTION GUARANTEED Walgreens.com © 2017 walgreen.com †Walgreens Pharmacist Survey *This product is not manufactured or distributed by Purdue Products L.P., owner of the registered trademark COLACE ® .

IMPORTANT: Keep this carton for future reference on full labeling. Walgreens Stool Softner DOCUSATE SODIUM

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 Walgreens Stool Softener Fruit Punch (this brand).

Top reported reactions

Nausea1,624
Fatigue1,592
Dyspnoea1,396
Constipation1,226
Diarrhoea1,226
Vomiting1,192
Pain1,170

Age at onset

Neonate10
Infant19
Child23
Adolescent33
Adult1,419
Elderly1,751

Reporter sex

0 reports
Male · 43%
Female · 57%
Unknown · 0%

Serious outcomes

Hospitalization9,622
Death2,786
Life-threatening1,214
Disabling800
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 1,736 679
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) — 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 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 WALGREENS CO.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
WALGREENS CO. 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.
← 00363-7131-25 · Walgreens 00363-7151-15 · WALGREENS →
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.