SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE
- Product NDC
- 10572-012
- 11-digit product format
- 105720012
- Labeler code
- 10572
- Product ID
- 10572-012_6ea7a63a-4e7e-4e24-a067-968bd91bb317
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium sulfate, potassium sulfate, magnesium sulfate
- Dosage form
- SOLUTION, CONCENTRATE
- Route
- ORAL
- Labeler
- Affordable Pharmaceuticals, LLC
- Application
- NDA022372
- Marketing category
- NDA
- Marketing start
- 2010-08-05
- Substance
- MAGNESIUM SULFATE, UNSPECIFIED FORM; POTASSIUM SULFATE; SODIUM SULFATE
- Active strength
- 1.6; 3.13; 17.5 g/mL; g/mL; g/mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MAGNESIUM SULFATE, UNSPECIFIED FORM | 1.6 g/mL |
| POTASSIUM SULFATE | 3.13 g/mL |
| SODIUM SULFATE | 17.5 g/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0YPR65R21J, 1K573LC5TV, DE08037SAB |
| Rxcui | 1001689, 1120068, 2390767 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10572-012-01 | SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE | 177.4 mL in 1 BOTTLE, PLASTIC | SOLUTION, CONCENTRATE | 177.4 | | 2 |
| 10572-012-01 | SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE | 2 in 1 CARTON | SOLUTION, CONCENTRATE | 2 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10572-012 | SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE (SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE) SOLUTION, CONCENTRATE [AFFORDABLE PHARMACEUTICALS, LLC] | 1 | Current NDC, Legacy NDC, 2 package rows | 20220706_f86bdcc8-e643-4160-89ae-01c89bee842d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10572-012-01 | 10572001201 | 2 BOTTLE, PLASTIC in 1 CARTON (10572-012-01) / 177.4 mL in 1 BOTTLE, PLASTIC | 2010-08-05 | 0000-00-00 | No | No | Current |