ANTACID MINT aluminum hydroxide, magnesium hydroxide, dimethicone 200 mg/5mL; 200 mg/5mL; 20 mg/5mL Suspension, 355 mL — NDC 63868-694-57 (Billing 63868-0694-57)
This is a package of 355 mL of ANTACID MINT aluminum hydroxide, magnesium hydroxide, dimethicone 200 mg/5mL; 200 mg/5mL; 20 mg/5mL Suspension from Chain Drug Marketing Association, marketed since Mar 2014 and currently FDA-listed, this package's marketing is listed to end Jul 2028; retail pharmacies pay about $0.0107 per mL (NADAC). It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 63868-694-57 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 63868 labeler · 694 product · 57 package
- Package marketed since
- Mar 1, 2014
- Package marketing ended
- Jul 31, 2028
- Sample package
- No — commercial package
- Billing quantity
- 355 mL per package
- Barcode (UPC-A, from the NDC)
- 3 6386869457 7
- FDA record last changed
- Oct 1, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
- GSN (GCN sequence number): 002701
- GCN: 63910
- HICL (First Databank): 001168
- AHFS class code: 56:04.00.00
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 3, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
Aluminum Hydroxide, Magnesium Hydroxide are antacids used together to relieve heartburn, acid indigestion, and upset stomach. They may be used to treat these symptoms in patients with peptic ulcer, gastritis, esophagitis, hiatal hernia, or too much acid in the stomach (gastric hyperacidity). They combine with stomach acid and neutralize it. Aluminum Hydroxide, Magnesium Hydroxide are available without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Read the full MedlinePlus article ↗Antacid Mint is an over-the-counter oral suspension containing aluminum hydroxide and magnesium hydroxide, which are antacid compounds typically used to neutralize stomach acid and relieve heartburn and indigestion. The suspension also contains dimethicone, an anti-gas agent commonly included to help reduce bloating and gas discomfort. This product is marketed under the FDA's over-the-counter monograph rules for antacid formulations.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 3, 2026
Ask a licensed pharmacist directly — free, answered by our team.
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 mL | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | $0.011 | $3.80 / 355 ml |
| 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. | |
Where does this data come from?
- CMS NADAC weekly file · file of Nov 23, 2022
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 5, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 63868-0694-57 You're viewing this Main listing | 355 mL in 1 BOTTLE | 2014-03-01 | Jul 31, 2028 | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file · file of Nov 23, 2022
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
What it looks like
Where does this data come from?
- FDA label on DailyMed · label index refreshed Oct 3, 2026
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 LKG8494WBH
Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
-
UNII 3QPI1U3FV8
A preservative derived from benzoic acid that prevents bacterial and fungal growth in medicines. It helps extend shelf life and maintain product safety during storage and use.
-
UNII K679OBS311
Carboxymethylcellulose sodium is a plant-derived thickening agent made from cellulose. In medicines, it acts as a binder to hold ingredients together, a disintegrant to help the tablet break apart, or a thickener in liquids.
-
UNII OP1R32D61U
Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
-
UNII 3NXW29V3WO
Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
-
UNII Z8IX2SC1OH
Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
-
UNII SB8ZUX40TY
Saccharin sodium is an artificial sweetener made from saccharin salt. It's added to medicines to improve taste, especially in liquid formulations for children or bitter drugs.
-
UNII 8KW3E207O2
A liquid sweetener made from sorbitol, a sugar alcohol derived from glucose. It sweetens the medicine and also acts as a humectant to help retain moisture and improve texture in liquid formulations.
-
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
9 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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.- FDA label on DailyMed · label index refreshed Oct 3, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from Chain Drug Marketing Association labeler code 63868
- Allergy Relief loratadine 10 mg Capsule, Liquid Filled NDC 63868-669-10
- OXYMETAZOLINE HYDROCHLORIDE .05 g/100mL Spray NDC 63868-676-01
- ACETAMINOPHEN 160 mg/5mL Suspension NDC 63868-677-60
- ACETAMINOPHEN 160 mg/5mL Suspension NDC 63868-678-60
- 8 Hour Pain Relief Acetaminophen 650 mg Tablet, Extended Release NDC 63868-679-50
- Stomach Relief Bismuth Subsalicylate 262 mg Tablet NDC 63868-691-40
- Quality Choice Infants Dye Free Gas Relief Simethicone 20 mg/.3mL Emulsion NDC 63868-696-30
- Quality Choice Phenylephrine Hydrochloride 1 g/100mL Solution/ Drops NDC 63868-697-30
- Quality Choice Maximum Strength oxymetazoline hydrochloride .05 g/100mL Spray NDC 63868-698-30
- Quality Choice Oxymetazoline Hydrochloride .05 g/100mL Spray NDC 63868-699-22
- Quality Choice Regular Strength Peppermint Flavor Calcium Carbonate 500 mg Tablet, Chewable NDC 63868-700-15
- Quality Choice Antacid Assorted Fruit Calcium Carbonate 500 mg Tablet, Chewable NDC 63868-701-66
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses relieves heartburn sour stomach acid indigestion the symptoms referred to as gas
⏱️ Dosage and Administration ▾
Directions • shake well before each use • adults and children 12 years and older: take 2 to 4 teaspoonfuls, as needed, up to four times a day, or as directed by a doctor • do not take more than 16 teaspoonfuls in 24 hours unless directed by a doctor or use the maximum dosage for more than 2 weeks • children under 12 years: ask a doctor
⚠️ Warnings ▾
Warnings 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 ▾
Other information • each 5 mL teaspoonful contains: magnesium 85 mg, sodium 3 mg • store at room temperature • protect from freezing • keep tightly closed
🧪 Active Ingredient ▾
Active ingredients (in each 5 mL teaspoonful) Aluminum hydroxide 200 mg (equivalent to dried gel, USP) Magnesium hydroxide 200 mg Simethicone 20mg
🧪 Inactive Ingredients ▾
Inactive ingredients benzyl alcohol, butylparaben, carboxymethylcellulose sodium, flavor, hypromellose, microcrystalline cellulose, propylparaben, purified water, saccharin sodium, sorbitol solution
🎯 Purpose ▾
Purposes Antacid Antigas
📄 Keep Out of Reach of Children ▾
Keep out of reach of children.
📄 Package Label / Principal Display Panel ▾
package Label 1