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Saline Laxative Cherry Laxative Sodium Phosphate, Dibasic and Sodium Phosphate, Monobasic, Unspecified Form 2.7 g/45mL; 7.2 g/45mL Liquid — NDC 55910-339-24 (Billing 55910-0339-24)

by Dolgencorp Inc. · 1 BOTTLE in 1 CARTON / 45 mL in 1 BOTTLE

This is a package of Saline Laxative Cherry Laxative Sodium Phosphate, Dibasic and Sodium Phosphate, Monobasic, Unspecified Form 2.7 g/45mL; 7.2 g/45mL Liquid from Dolgencorp Inc., marketed since Mar 2016 and currently FDA-listed. It is this product's only package size.

NDC 55910-0339-24
🏷️ FDA NDC (as labeled) 55910-339-24 billing pads the product 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) 55910-339-24
Product NDC 55910-339
11-digit billing NDC 55910033924
RxCUI 1604338
UNII GR686LBA74, 3980JIH2SW
UPC 0838891010446
Application # part334
SPL Set ID ca3c00d9-4301-4de8-94f5-34f1bcc761ab
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH NOT FINAL
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-03-15
Route ORAL
Dosage form LIQUID
Substance SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM
Quick answers
  • RxCUI (RxNorm): 1604338
Why two NDCs? The FDA registers this code as 55910-339-24 — 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 → 55910-0339-24. 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.

Clinical

🧪 What is this product?

This is an over-the-counter oral liquid laxative product containing sodium phosphate salts (dibasic and monobasic forms). Sodium phosphate is commonly used as a saline laxative, meaning it works by drawing water into the bowel to help promote bowel movements. This product is marketed under the FDA's OTC monograph rules for laxatives rather than as an individually approved drug application. The cherry flavoring is added for taste.

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 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
55910-0339-24 You're viewing this Main listing 1 BOTTLE in 1 CARTON / 45 mL in 1 BOTTLE 2016-03-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Saline Laxative Cherry Laxative 2.7 g/45mL; 7.2 g/45mLthis 55910-0339-24 Dolgencorp 1 bottle — — 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

🏛️
2016
On the market since
Mar 2016
📍
2026
Currently FDA-listed
10 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

LabelerDolgencorp Inc.
FDA applicationpart334 (OTC MONOGRAPH NOT FINAL)
Labeler code55910
First marketedMar 2016
Product typeHuman Otc Drug
Portfolio3 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 6 words ▾

Use for relief of occasional constipation

⏱️ Dosage and Administration 137 words ▾

Directions Use as a laxative for relief of occasional constipation dilute dose in the table below with one glass (8 fl. oz.) of cool water. Drink, then follow with at least one additional glass (8 fl. oz.) of cool water. There is significant loss of liquid when using this product.

To prevent dehydration, drink plenty of clear liquid after use. do not use for bowel cleansing there are three teaspoons in one tablespoon do not take more unless directed by a doctor. See Warnings . Ages (years) Dosage Maximum Dose 12 & older 1 Tablespoon 2 or 3 Tablespoons SINGLE DAILY DOSAGE.

DO NOT TAKE MORE OF THIS PRODUCT IN A 24-HOUR PERIOD 10 & 11 1 Tablespoon 1 Tablespoon 5 to 9 1 ½ Teaspoons 1 ½ Teaspoons Under 5 Do Not Use Do Not Use

⚠️ Warnings ~1 min read ▾

Warnings Dosage Warning Taking more than the recommended dose in 24 hour can be harmful. Do not use if you have a previous kidney problem, congestive heart failure, impaired renal functions, decreased intervascular volume, dehydration, uncorrected electrolyte abnormalities in children under 5 years old for bowel cleansing Ask a doctor before use if you have abdominal pain, nausea, or vomiting kidney disease heart problems a sudden change in bowel habits lasting more than 2 weeks already used a laxative for more than a week dehydration Ask a doctor or pharmacist before use if you are on a sodium restricted diet under a doctor's care for any medical condition taking any other prescription or non-prescription medications.

Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work. Stop use and ask a doctor if you have any rectal bleeding do not have a bowel movement within 6 hours have any symptoms that your body is losing more fluid than you are drinking have symptoms of dehydration including thirstiness dizziness urinating less often than normal vomiting These symptoms may indicate a serious condition.

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: 800-222-1222.

📦 Storage and Handling 49 words ▾

Other information Each Tablespoon contains: sodium 1.6 g Saline laxatives increase retention of water in the intestines, promoting bowel movements. this product generally produces a bowel movement in 30 minutes to 6 hours this product is sugar free do not freeze store at 15 to 30°C (59 to 86°F)

🧪 Active Ingredient 20 words ▾

Active ingredients (in each tablespoon) Purpose Dibasic sodium phosphate 2.7 g/tablespoon. Saline laxative Monobasic sodium phosphate 7.2 g/tablespoon Saline laxative

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients Cherry flavor, glycerin, purified water, saccharin sodium, sodium benzoate

🎯 Purpose 20 words ▾

Active ingredients (in each tablespoon) Purpose Dibasic sodium phosphate 2.7 g/tablespoon. Saline laxative Monobasic sodium phosphate 7.2 g/tablespoon Saline laxative

📄 Do Not Use 32 words ▾

Do not use if you have a previous kidney problem, congestive heart failure, impaired renal functions, decreased intervascular volume, dehydration, uncorrected electrolyte abnormalities in children under 5 years old for bowel cleansing

📄 Ask a Doctor Before Use If 38 words ▾

Ask a doctor before use if you have abdominal pain, nausea, or vomiting kidney disease heart problems a sudden change in bowel habits lasting more than 2 weeks already used a laxative for more than a week dehydration

📄 Ask a Doctor or Pharmacist Before Use If 49 words ▾

Ask a doctor or pharmacist before use if you are on a sodium restricted diet under a doctor's care for any medical condition taking any other prescription or non-prescription medications. Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work.

📄 Stop Use and Ask a Doctor If 55 words ▾

Stop use and ask a doctor if you have any rectal bleeding do not have a bowel movement within 6 hours have any symptoms that your body is losing more fluid than you are drinking have symptoms of dehydration including thirstiness dizziness urinating less often than normal vomiting These symptoms may indicate a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

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

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away: 800-222-1222.

📄 Package Label / Principal Display Panel 44 words ▾

PRINCIPAL DISPLAY PANEL - 45 mL Bottle Carton ◀ FOR DIRECTIONS LIFT SIDE PANEL NDC 55910-339-24 Since 1903 Rexall ® Oral Saline Laxative Phosphate For Relief of: Occasional Constipation Cherry Splash

1.5 FL OZ (45 mL) PRINCIPAL DISPLAY PANEL - 45 mL Bottle Carton

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) — 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 Not Final". 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 Dolgencorp Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Dolgencorp 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.
← 55910-0336-09 · Dolgencorp, 55910-0340-24 · Dollar →
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.