Indications and uses
relieves occasional constipation (irregularity) generally produces bowel movement in 1/2 to 6 hours
relieves occasional constipation (irregularity) generally produces bowel movement in 1/2 to 6 hours
shake well before use do not exceed the maximum recommended daily dose in a 24 hour period dose may be taken once a day preferably at bedtime, in divided doses, or as directed by a doctor follow each dosage with a full glass (8 oz) of liquid age dose adults and children 12 years and over 30 mL to 60 mL children 6 to 11 years 15 mL to 30 mL children under 6 years ask a doctor
each 15 mL contains: magnesium 500 mg, sodium 6 mg do not freeze store at room temperature tightly closed
Magnesium hydroxide 1200 mg
Saline laxative
Ask a doctor before use if you have
Ask a doctor or pharmacist before use if you are presently taking a prescription drug.
This product may interact with certain prescription drugs.
Stop use and ask a doctor if
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 (1-800-222-1222) right away.
| age | dose |
| adults and children 12 years and over | 30 mL to 60 mL |
| children 6 to 11 years | 15 mL to 30 mL |
| children under 6 years | ask a doctor |
carboxymethylcellulose sodium, citric acid, D & C red no. 28, flavor, glycerin, microcrystalline cellulose, purified water, sodium citrate, sodium hypochlorite, sucrose, xanthan gum
1-800-540-3765
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70000-0064 | MILK OF MAGNESIA (MAGNESIUM HYDROXIDE) SUSPENSION [CARDINAL HEALTH] | 4 | Legacy NDC | 20231108_af5f681e-a306-0cbc-e053-2995a90a63ba.zip |
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70000-0064-1 | ML - Milliliter | 70000-0064 | d8c9c924-1d37-49df-b40e-aaf860f5f443 | 1 | 2021-06-02 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 70000-0064 | 70000-0064-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| D&C RED NO. 28 | 767IP0Y5NH | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM HYPOCHLORITE | DY38VHM5OD | IACT |
| MAGNESIUM HYDROXIDE | NBZ3QY004S | ACTIB |
| SUCROSE | C151H8M554 | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM | K679OBS311 | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 3c42084a-1bb5-1377-e063-6294a90a69a4 | af5f681e-a306-0cbc-e053-2995a90a63ba | 2025-08-13 | Warnings | af5f681e-a306-0cbc-e053-2995a90a63ba |
Adverse event summaries are temporarily unavailable. Other product information remains available.