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ENEMEEZ DOCUSATE SODIUM 283 mg/5mL Liquid — NDC 17433-9876-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ENEMEEZ DOCUSATE SODIUM 283 mg/5mL Liquid — NDC 17433-9876-2 (Billing 17433-9876-02)

by Quest Products, LLC · 2 TUBE in 1 CONTAINER / 5 mL in 1 TUBE

This is a package of ENEMEEZ DOCUSATE SODIUM 283 mg/5mL Liquid from Quest Products, LLC, marketed since Jun 2012 and currently FDA-listed.

NDC 17433-9876-02
🏷️ FDA NDC (as labeled) 17433-9876-2 billing pads the package segment with a zero
This package
Contains5 mL in 1 tube Pack sizes7 compare ↓
Product page 17433-9876-03 Also comes in: 5 mL 17433-9876-1 5 tubes 17433-9876-5 6 tubes 17433-9876-6 30 tubes 17433-9876-3 35 tubes 17433-9876-9 65 tubes 17433-9876-4
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ 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 →

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 17433-9876-2 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
17433 labeler · 9876 product · 2 package
Package marketed since
Jan 26, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 1743398762 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 17433-9876-2
Product NDC 17433-9876
11-digit billing NDC 17433987602
NCPDP billing unit ML — per mL (volume)
RxCUI 1190184, 1192923
UNII F05Q2T2JA0
Application # M007
SPL Set ID 0b06445d-0839-497e-bdff-e0fe224a7738
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2012-06-15
Route RECTAL
Dosage form LIQUID
Substance DOCUSATE SODIUM

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 46500010305110
GCN Seq No 068187
GCN 30916
HICL code 001326
Ingredient (HICL) Docusate Sodium
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q3
Therapeutic class — intermediate (HIC2) Anal-Rectal Preparations
HIC3 code Q3S
Therapeutic class — specific (HIC3) Laxatives, Local/Rectal
AHFS code 56:12.00.00
AHFS class Cathartics And Laxatives
FDB label name ENEMEEZ MINI ENEMA
FDB brand name Enemeez
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 068187
  • GCN: 30916
  • GPI-14 (Medi-Span): 46500010305110
  • HICL (First Databank): 001326
  • AHFS class code: 56:12.00.00
  • RxCUI (RxNorm): 1190184
Why two NDCs? The FDA registers this code as 17433-9876-2 — 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 → 17433-9876-02. 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 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

Label name ENEMEEZ MINI ENEMA Ingredient Docusate Sodium
🧪 What is this product?

Enemeez Docusate Sodium is an over-the-counter rectal liquid containing the active ingredient docusate sodium. Docusate sodium is a stool softener typically used to relieve constipation by helping water mix into stool to make bowel movements easier. This product is marketed as an OTC monograph drug, meaning it follows established FDA rules for its category rather than going through individual product 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.
Try another pack size: 5 mL 5 tubes 6 tubes 30 tubes 35 tubes 65 tubes
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 Per unit Per pack Marketing startMarketing endStatus
17433-9876-03 17433-9876-3 Main listing 30 TUBE in 1 CONTAINER / 5 mL in 1 TUBE $0.3665 / mL $54.97 2012-06-15 — Active
17433-9876-05 17433-9876-5 5 TUBE in 1 CONTAINER / 5 mL in 1 TUBE $0.4079 / mL $10.20 2022-01-14 — Active
17433-9876-09 17433-9876-9 35 TUBE in 1 CONTAINER / 5 mL in 1 TUBE — — 2021-10-08 — Active
17433-9876-06 17433-9876-6 6 TUBE in 1 CONTAINER / 5 mL in 1 TUBE — — 2023-09-14 — Active
17433-9876-01 17433-9876-1 1 TUBE in 1 CONTAINER / 5 mL in 1 TUBE Sample — — 2025-04-28 — Active
17433-9876-02 You're viewing this 2 TUBE in 1 CONTAINER / 5 mL in 1 TUBE — — 2024-01-26 — Active
17433-9876-04 17433-9876-4 65 TUBE in 1 CONTAINER / 5 mL in 1 TUBE — — 2026-06-30 — Active

This pack shows little to no recent Medicaid volume — a different pack size carries most fills. See all packs ↓

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 2 tube in 1 container / 5 ml in 1 tube.
What NDC number is used to bill for this package of ENEMEEZ DOCUSATE SODIUM 283 mg/5mL Liquid?
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.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Docusate Mini Enema 283 mg/5mL 00904-6920-93 Major 30 tubes $0.461 — Availability likely —
Enemeez 283 mg/5mLthis 17433-9876-02 Quest 2 tubes — — 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

🏛️
2012
On the market since
Jun 2012
📍
2026
Currently FDA-listed
14 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 5655G9Y8AQ
    A synthetic liquid polymer used as a solvent and humectant in medications. It helps dissolve active ingredients, maintain moisture in the formulation, and improve how the medicine flows and is absorbed.

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

The official label also statesGlycerin USP and Polyethylene Glycol

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

LabelerQuest Products, LLC
FDA applicationM007 (OTC MONOGRAPH DRUG)
Labeler code17433
First marketedJun 2012
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from Quest Products, LLC labeler code 17433

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 19 words ▾

Uses For relief of occasional constipation (irregularity). This product generally produces a bowel movement in 2 to 15 minutes.

⏱️ Dosage and Administration 173 words ▾

Directions Adults and children 12 years of age and older (with adult supervision) one to three units daily. Children under 12 years of age, consult a doctor prior to use. Twist off and remove tip.

Lubricate tip prior to insertion: Place a few drops of the tube's liquid content on the shaft prior to insertion. Also apply liquid content or lubricant to the anus before inserting the mini-enema. Positioning: For best results, lay on left side with knees bent.

Insert slowly into rectum, up to the shoulder of tube. Alternate positions: Administer while seated on the toilet. Or, kneel, then lower head and chest forward until side of face is resting on the surface.

With steady pressure, gently insert the tube into the rectum with care to prevent damage to the rectal wall. Squeeze to empty the contents. Keep the tube squeezed until it is removed from the rectum.

After the contents have been emptied, remove the disposable tube and discard. A small amount of liquid may remain in the unit after use.

⚠️ Warnings 25 words ▾

Warnings For rectal use only. Drug Interaction Precaution: Do not take this product if you are presently taking mineral oil, unless directed by a doctor.

📦 Storage and Handling 12 words ▾

Other Information Other Information Store at room temperature 15°-30° C (59°-86° F)

🧪 Active Ingredient 12 words ▾

Drug Facts Active ingredient (per delivered dose) Docusate Sodium USP 283 mg

🧪 Inactive Ingredients 7 words ▾

Inactive Ingredients Glycerin USP and Polyethylene Glycol

🎯 Purpose 4 words ▾

Purpose Stool Softener Laxative

📄 Do Not Use 27 words ▾

Do not use Laxative products when abdominal pain, nausea or vomiting are present. Laxative products for a period longer than 1 week unless directed by a doctor.

📄 Stop Use and Ask a Doctor If 40 words ▾

Stop use and ask a doctor if you have: Rectal bleeding. Noticed a sudden change in bowel habits that persists over a period of 2 weeks Failed to have a bowel movement after use. This may indicate a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

Pregnant or Lactating Women, ask a healthcare professional before use.

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

📄 Questions or Comments 23 words ▾

Questions or Comments: (888) 273-9734 or www.enemeez.com Manufactured by: Summit Pharmaceuticals, Inc. Phoenix, AZ 85027 Distributed by: Alliance Labs, LLC. Phoenix, AZ 85027

📄 Package Label / Principal Display Panel 5 words ▾

Principal Display Panels: 9876-5 30count

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicaid utilization by pack size

Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
30 tubes17433-9876-03 15,043 Rx · $1,023,203
5 tubes17433-9876-05 530 Rx · $28,055
35 tubes17433-9876-09 No Medicaid data
6 tubes17433-9876-06 No Medicaid data
1 tube17433-9876-01 No Medicaid data
2 tubes this page17433-9876-02 No Medicaid data
65 tubes17433-9876-04 No Medicaid data
Drug total (last 4 qtrs): 15,573 Rx · 2,424,743 units · $1,051,258 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.

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 DOCUSATE SODIUM — the ingredient across all brands.

Top reported reactions

Fatigue5,208
Nausea4,926
Dyspnoea3,840
Diarrhoea3,794
Constipation3,749
Death3,437
Pain3,409

Age at onset

Neonate16
Infant27
Child48
Adolescent69
Adult3,781
Elderly4,473

Reporter sex

61,438 reports
Male · 41%
Female · 59%
Unknown · 0%

Serious outcomes

Hospitalization26,723
Life-threatening2,579
Disabling1,817
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 4,713 0
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 Quest Products, LLC. 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 6 other package presentations of this same product, including 1 tube (17433-9876-01), 5 tubes (17433-9876-05), 6 tubes (17433-9876-06). 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?
Quest Products, 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.
← 17404-1035-01 · Farmhispania 17433-9877-03 · Quest →
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.