Magnesium phosphoricum 6X
- Product NDC
- 48951-7220
- 11-digit product format
- 489517220
- Labeler code
- 48951
- Product ID
- 48951-7220_36eb354c-9178-0d49-e063-6294a90ab28d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Magnesium phosphoricum 6x
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- MAGNESIUM PHOSPHATE
- Active strength
- 6 [hp_X]/g
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Magnesium phosphoricum 6X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MAGNESIUM PHOSPHATE | 6 [hp_X]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 453COF7817 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7220-4 | Magnesium phosphoricum 6X | 50 g in 1 BOTTLE, GLASS | POWDER | 50 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-7220-4 | 48951722004 | 50 g in 1 BOTTLE, GLASS (48951-7220-4) | 50 g | 2009-09-01 | No | No | Current |