Home › NDC Lookup › Ingredients › Aluminum Hydroxide, Magnesium Hydroxide,... › 11822-3727-06
🧴image loading
(from DailyMed)

MAXIMUM STRENGTH ANTACID AND GAS RELIEF aluminum hydroxide, magnesium hydroxide, dimethicone 400 mg/5mL; 400 mg/5mL; 40 mg/5mL Suspension, 355 mL — NDC 11822-3727-6 (Billing 11822-3727-06)

by RITE AID PHARMACY · 355 mL in 1 BOTTLE

This is a package of 355 mL of MAXIMUM STRENGTH ANTACID AND GAS RELIEF aluminum hydroxide, magnesium hydroxide, dimethicone 400 mg/5mL; 400 mg/5mL; 40 mg/5mL Suspension from RITE AID PHARMACY, no longer marketed (first marketed Apr 2014), no longer in the FDA NDC Directory, this package's marketing ended Sep 2026. It is this product's only package size.

NDC 11822-3727-06
🏷️ FDA NDC (as labeled) 11822-3727-6 billing pads the package segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Sep 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 11822-3727-6
Product NDC 11822-3727
11-digit billing NDC 11822372706
RxCUI 237870
UNII 5QB0T2IUN0, NBZ3QY004S, 92RU3N3Y1O
Application # M001
SPL Set ID 6014342d-ad46-ae71-e053-2991aa0a8929
Physiologic effect Skin Barrier Activity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Sep 2026)
Marketing start 2014-04-01
Marketing end 2026-09-30
Route ORAL
Dosage form SUSPENSION
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE

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

GPI-14 49200020100305
GPI class RA Acid Reducer Max St
Quick answers
  • GPI-14 (Medi-Span): 49200020100305
  • RxCUI (RxNorm): 237870
Why two NDCs? The FDA registers this code as 11822-3727-6 — 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 → 11822-3727-06. 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 Aluminium compounds class.

Drug family (ATC) Aluminium compounds
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 oral suspension that combines two antacids with an anti-gas agent. Aluminum hydroxide and magnesium hydroxide are commonly used to neutralize stomach acid and provide relief from heartburn and indigestion. Dimethicone functions as an anti-foaming agent and is typically included to help reduce gas and bloating. This product is marketed as an OTC monograph drug, meaning it follows FDA's established safety and effectiveness guidelines for antacid and anti-gas products.

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
11822-3727-06 You're viewing this Main listing 355 mL in 1 BOTTLE 2014-04-01 Sep 30, 2026 Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Maximum Strength Antacid 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 63868-0715-57 Chain 355 ml $0.010 — FDA listed —
Almacone Double Strength 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 00536-0015-83 RUGBY 355 ml $0.012 — Availability likely —
Mintox Maximum Strength 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 00904-5725-14 MAJOR 355 ml $0.012 — Availability likely —
Antacid Antigas Nta 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 46122-0431-40 AMERISOURCEBERGEN 355 ml $0.012 — Availability likely —
Antacid Antigas Nta 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 46122-0432-40 AMERISOURCEBERGEN 355 ml $0.012 — Availability likely —
Maximum Strength Antacid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 70000-0062-01 CARDINAL 355 ml $0.012 — Availability likely —
Maximum Strength Antacid 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 70000-0422-01 CARDINAL 355 ml $0.012 — Availability likely —
Maximum Strength Antacid Antigas 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 70677-1064-01 STRATEGIC 355 ml $0.012 — Availability likely —
Maximum Strength Antacid And Antigas 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 70677-1065-01 STRATEGIC 355 ml $0.012 — Availability likely —
QCH Maximum Strength Antacid 516 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 83324-0122-12 Chain 355 ml $0.012 — Availability likely —
Mag-AL Plus XS 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 00121-1762-30 PAI 10 cups — — FDA listed —
Maximum Strength Antacid Antigas 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 00363-1691-12 WALGREEN 355 ml — — FDA listed —
Maximum Strength Antacid And Gas Relief 400 mg/5mL; 400 mg/5mL; 40 mg/5mLthis 11822-3727-06 RITE 355 ml — — Discontinued —
Maximum Strength Antacid And Antigas 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 11822-5742-00 RITE 355 ml — — Discontinued —
Mintox Maximum Strength 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 17856-5725-03 ATLANTIC 30 ml — — FDA listed —
Antacid 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 21130-0508-05 Safeway 177 ml — — FDA listed —
Antacid Plus 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 21130-0691-12 BETTER 355 ml — — FDA listed —
Maximum Strength Antacid 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 30142-0638-12 KROGER 355 ml — — FDA listed —
Maximum Strength Antacid Mint 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 36800-0342-40 Topco 355 ml — — FDA listed —
Maximum Strength Antacid Cherry liquid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 36800-0587-40 Topco 355 ml — — FDA listed —
maximum strength antacid cherry 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 41163-0065-05 UNITED 355 ml — — FDA listed —
Maximum Strength Antacid Cherry 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 49035-0638-12 WAL-MART 355 ml — — FDA listed —
Maximum Strength Antacid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 49035-0681-12 WAL-MART 355 ml — — FDA listed —
Maximum Strength Antacid And Gasrelief 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 50804-0619-12 GOODSENSE 355 ml — — FDA listed —
Antacid And Gasrelief 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 50804-0638-12 GOODSENSE 355 ml — — FDA listed —
Maximum Strength Antacid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 51316-0142-12 CVS 355 ml — — FDA listed —
Mag-Al Plus XS 2400 mg/30mL; 2400 mg/30mL; 240 mg/30mL 55154-9422-05 Cardinal 5 cups — — FDA listed —
Maximum Strength Advanced Antacid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 55910-0638-12 DOLGENCORP, 355 ml — — FDA listed —
Aluminum Hydroxide, Magnesium Hydroxide and Simethicone 2400 mg/30mL; 2400 mg/30mL; 240 mg/30mL 57237-0324-31 Rising 100 cups — — FDA listed —
Geri-Lanta Maximum Strength 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 57896-0619-12 Geri-Care 355 ml — — FDA listed —
Geri-Mox Max Cherry 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 57896-0638-10 Geri-Care 100 cups — — FDA listed —
MAXIMUM STRENGTH Antacid 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 57896-0664-12 Geri-Care 355 ml — — FDA listed —
Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 60687-0888-76 American 10 cups — — FDA listed —
Mylanta Maximum Strength Classic Flavor 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 62372-0500-12 Infirst 355 ml — — FDA listed —
Mylanta Maximum Strength Vanilla Caramel Flavor 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 62372-0504-12 Infirst 355 ml — — FDA listed —
Maximum Strength Antacid And Antigas 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 63941-0619-12 VALU 355 ml — — FDA listed —
Maximum Strength Antacid And Antigas Cherry 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 63941-0638-12 VALU 355 ml — — FDA listed —
Geri-Lanta Maximum Strength 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 68071-3423-01 NuCare 355 ml — — FDA listed —
Mintox Maximum Strength 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 68071-4114-01 NuCare 355 ml — — FDA listed —
Maximum Strength Antacid Cherry 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 69256-0508-40 Harris 355 ml — — FDA listed —
Maximum Strength Antacid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 69256-0517-05 Harris 355 ml — — FDA listed —
Maximum Strength Antacid Mint 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 69842-0296-73 CVS 355 ml — — FDA listed —
Antacid 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 69842-0508-05 CVS 355 ml — — FDA listed —
Maximum Strength Antacid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 69842-0619-12 CVS 355 ml — — FDA listed —
Maximum Strength Antacid Cherry 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 69842-0683-12 CVS 355 ml — — Discontinued —
Mintox Maximum Strength 400 mg/5mL; 400 mg/5mL; 40 mg/5mL 71205-0515-35 Proficient 355 ml — — FDA listed —
Antacid 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 72476-0516-05 Retail 355 ml — — FDA listed —
Maximum Strength Antacid and Antigas 800 mg/10mL; 800 mg/10mL; 80 mg/10mL 79481-0638-01 Meijer, 355 ml — — FDA listed —
Kesin MAG-AL Plus XS 40 mg/5mL; 400 mg/5mL; 400 mg/5mL 81033-0007-01 Kesin 100 cups — — FDA listed —
Aluminum Hydroxide, Magnesium Hydroxide and Simethicone 2400 mg/30mL; 2400 mg/30mL; 240 mg/30mL 84415-0010-01 Everpharm 100 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

🏛️
2014
On the market since
Apr 2014
📍
2026
Currently FDA-listed
12 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

LabelerRITE AID PHARMACY
FDA applicationM001 (OTC MONOGRAPH DRUG)
Labeler code11822
First marketedApr 2014
Product typeHuman Otc Drug
Portfolio7 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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Uses relieves heartburn sour stomach acid indigestion the symptoms referred to as gas

⏱️ Dosage and Administration 34 words ▾

Directions shake well before use adults and children 12 years and older: take 2 to 4 teaspoonfuls between meals, at bedtime, or as directed by a doctor children under 12 years: ask a doctor

⚠️ Warnings 86 words ▾

Warnings Do not take more than 12 teaspoonfuls in a 24 hour period or use the maximum dosage for more than 2 weeks Ask a doctor before use if you have kidney disease a magnesium-restricted diet Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs. Stop use and ask a doctor if symptoms last more than 2 weeks If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

📦 Storage and Handling 23 words ▾

Other information each 5 mL teaspoonful contains: magnesium 165 mg, sodium 5 mg protect from freezing store at room temperature keep tightly closed

🧪 Active Ingredient 22 words ▾

Active ingredients (in each 5 mL teaspoonful) Aluminum hydroxide 400 mg (equivalent to dried gel, USP) Magnesium hydroxide 400 mg Simethicone 40mg

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients benzyl alcohol, butylparaben, carboxymethylcellulose sodium, flavor (contains alcohol), hypromellose, microcrystalline cellulose, propylparaben, purified water, saccharin sodium, sorbitol solution

🎯 Purpose 3 words ▾

Purposes Antacid Antigas

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-540-3765

📄 Package Label / Principal Display Panel 3 words ▾

package Label 1

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 Aluminum hydroxide, magnesium hydroxide, dimethicone — the ingredient across all brands.

Top reported reactions

Burning Sensation1
Chest Pain1
Chromaturia1
Dizziness Postural1
Drug Interaction1
Dyspnoea1
Dysuria1

Reporter sex

6 reports
Male · 80%
Female · 20%

Serious outcomes

Hospitalization2
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 2 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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
RITE AID PHARMACY 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.
← 11822-3709-09 · Rite 11822-3775-07 · Rite →
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.