Magnesium Citrate
- Product NDC
- 51316-883
- 11-digit product format
- 513160883
- Labeler code
- 51316
- Product ID
- 51316-883_5c5155e4-f904-ddfd-e063-6394a90adae3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CVS Magnesium Citrate Oral Solution - Peach
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- CVS Pharmacy, Inc.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-25
- Substance
- MAGNESIUM CITRATE
- Active strength
- 1.745 g/29.6mL
- 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
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Magnesium Citrate
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MAGNESIUM CITRATE | 1.745 g/29.6mL |
openFDA label cross-check#
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 51316-883-10 | 51316088310 | 296 mL in 1 BOTTLE, PLASTIC (51316-883-10) | 296 ml | 2026-09-25 | No | No | Current |