Dulcolax Soft Chews Mixed Berry MAGNESIUM HYDROXIDE 1200 mg Tablet, Chewable, 90-count
by Chattem, Inc. · 90 TABLET, CHEWABLE in 1 BAG (41167-0265-2)
NDC 41167-0265-02
🏷️ FDA NDC (as labeled)
41167-0265-2
billing pads the package segment with a zero
This package
Contains90-count
Pack sizes4 compare ↓
OTC
On market
Non-controlled
🗂️ Data synced Sep 17, 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)
41167-0265-2
Product NDC
41167-0265
11-digit billing NDC
41167026502
RxCUI
2280709
UNII
NBZ3QY004S
Application #
M001
SPL Set ID
fe71907c-b1eb-4433-9337-933a944f3e62
Established class (EPC)
Calculi Dissolution Agent; Osmotic Activity
Mechanism of action
Magnesium Ion Exchange Activity
Physiologic effect
Increased Large Intestinal Motility; Inhibition Large Intestine Fluid/Electrolyte Absorption; Inhibition Small Intestine Fluid/Electrolyte Absorption
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-02-23
Route
ORAL
Dosage form
TABLET, CHEWABLE
Substance
MAGNESIUM HYDROXIDE
Why two NDCs?
The FDA registers this code as 41167-0265-2 — 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 → 41167-0265-02. 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 Magnesium compounds class.
Drug family (ATC)
Magnesium compounds, Other urologicals
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
LabelerChattem, Inc.
FDA applicationM001 (OTC MONOGRAPH DRUG)
Labeler code41167
First marketedFeb 2020
Product typeHuman Otc Drug
Portfolio157 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 it is MedlinePlus · NLM
Magnesium hydroxide is used to treat occasional constipation in children and adults on a short-term basis. Magnesium hydroxide is in a class of medications called saline laxatives. It works by causing water to be retained with the stool. This increases the number of bowel movements and softens the stool so it is easier to pass.
Read the full MedlinePlus article ↗📗 Our plain-language guide HelloPharmacist
- It depends on the product you pick up. Most magnesium hydroxide products — like Dulcolax liquid, Colace Fast-Acting Saline Laxative, MiraFAST soft chews, and many Milk of Magnesia...
- What is magnesium hydroxide actually used for?
- Yes, a few things matter here. If you're taking a liquid or suspension, shake it well before every use. Whatever form you take, follow it with a full 8-ounce glass of water or anot...
- How should I take it — does it matter when or how I drink it?
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Magnesium Hydroxide (OTC drug) — tap one for details:
3
Nutrient depletion considerations
Magnesium Hydroxide (OTC drug) may be associated with lower levels of 3 nutrients — worth a chat with your pharmacist, not a cause for alarm.
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.
💬 Questions about MAGNESIUM HYDROXIDE?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
pink
ShapeRectangle
Size25 mm
ScoringNot scored
FlavorBerry
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 each | 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 |
|---|---|---|---|---|---|---|
| Walgreens Blueberry Raspberry Gentle Laxative 1200 mg 00363-1099-30 | Walgreen | 30 tablets | — | — | FDA listed | — |
| Walgreens SmoothLAX Soft Chews 1200 mg 00363-9963-60 | Walgreens | 60 tablets | — | — | FDA listed | — |
| MiraFAST soft chews 1200 mg 11523-0159-01 | Bayer | 30 pouches | — | — | FDA listed | — |
| Dulcolax Soft Chews Watermelon 1200 mg 41167-0259-00 | Chattem, | 15 tablets | — | — | FDA listed | — |
| Dulcolax Soft Chews Mixed Berry 1200 mgthis 41167-0265-02 | Chattem, | 90 tablets | — | — | FDA listed | — |
| CVS Magnesium Hydroxide Laxative Chew 1200 mg 51316-0083-30 | CVS | 30 tablets | — | — | FDA listed | — |
| Meijer Magnesium Hydroxide Laxative Soft Chew 1200 mg 79481-0094-01 | Meijer | 30 tablets | — | — | FDA listed | — |
| Equate Gentle Laxative Soft chew 1200 mg 79903-0220-30 | Walmart | 30 tablets | — | — | FDA listed | — |
| Equate Kids Gentle Laxative SC 1200 mg 79903-0252-15 | Walmart | 15 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
🏛️
2020
On the market since
Feb 2020
📍
2026
Currently FDA-listed
6 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 Dulcolax Soft Chews Mixed Berry (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 36%
Female · 64%
Unknown · 0%
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 |
|---|---|---|---|
| 41167-0265-03 | 30 TABLET, CHEWABLE in 1 BAG (41167-0265-3) | 2020-02-23 | Active |
| 41167-0265-06 | 60 TABLET, CHEWABLE in 1 BAG (41167-0265-6) | 2020-02-23 | Active |
| 41167-0265-08 | 15 TABLET, CHEWABLE in 1 BAG (41167-0265-8) | 2021-01-01 | Active |
| 41167-0265-02 You're viewing this | 90 TABLET, CHEWABLE in 1 BAG (41167-0265-2) | 2026-04-01 | Active |
You're viewing the largest of 4 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 41167-0265-02?
NDC 41167-0265-02 is a 90-count package — 90 tablet, chewable in 1 bag.
What is the difference between NDC 41167-0265-02 and NDC 41167-0265-08?
Both are Dulcolax Soft Chews Mixed Berry MAGNESIUM HYDROXIDE 1200 mg Tablet, Chewable — the drug itself is identical. NDC 41167-0265-02 is the 90-count package, while NDC 41167-0265-08 is the 15 tablets package.
What NDC number is used to bill for this package of Dulcolax Soft Chews Mixed Berry MAGNESIUM HYDROXIDE 1200 mg Tablet, Chewable?
Bill NDC 41167-0265-02 — the 11-digit billing format is 41167026502. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 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 41167-0265-2, 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: 41167-0265-02, written without dashes as 41167026502. 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 41167-0265-02, the first segment (41167) is the labeler code FDA assigned to Chattem, Inc.; the middle segment (0265) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Chattem, Inc.. 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 3 other package presentations of this same product, including 15 tablets (41167-0265-08), 30 tablets (41167-0265-03), 60 tablets (41167-0265-06). 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?
Chattem, 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.
📄 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
🎯 Indications and Usage ▾
Use ● for relief of occasional constipation (irregularity) ● this product generally produces bowel movement in ½ to 6 hours
⏱️ Dosage and Administration ▾
Directions ● drink a full glass (8 oz) of liquid with each dose ● dose may be taken as a single daily dose or in divided doses ● do not exceed the maximum recommended daily dose in a 24 hour period adults and children 12 years of age and over take 2 to 4 chews children 6 to under 12 years of age take 1 to 2 chews children 4 to under 6 years of age take 1 chew (single dose or in divided doses) children under 4 years of age ask a doctor
⚠️ Warnings ▾
Warnings Ask a doctor before use if you have ● kidney disease ● a magnesium-restricted diet ● stomach pain, nausea or vomiting ● noticed a sudden change in bowel habits that lasts over 2 weeks Ask a doctor or p harmacist before use if you are taking a prescription drug. This product may interact with certain prescription drugs. Stop use and ask a doctor if ● you have rectal bleeding or fail to have a bowel movement after using this product.
These could be signs of a serious condition. ● you need to use a 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.
🧪 Active Ingredient ▾
Active ingredient (in each chew ) Magnesium hydroxide 1200 mg
🧪 Inactive Ingredients ▾
Inactive ingredients corn syrup, FD&C red no. 40, glycerin, hydrogenated coconut oil, lecithin (soy), natural flavor, sucrose, water
🎯 Purpose ▾
Purpose Saline laxative
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.