citroma
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- citroma
- Generic name
- MAGNESIUM CITRATE
- Manufacturer
- Target Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a8e52a22-7c30-40c0-8f78-523775743bfb
- SPL ID
- 4b1e3edc-e0f6-1af3-e063-6394a90a4a1b
- Version
- 18
- Effective date
- 2026-02-18
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:35:24
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M007 | openfda.application_number | |
| brand name | citroma | openfda.brand_name | |
| generic name | MAGNESIUM CITRATE | openfda.generic_name | |
| manufacturer name | Target Corporation | openfda.manufacturer_name | |
| ndc | package | 11673-708-38 | openfda.package_ndc |
| ndc | product | 11673-708 | openfda.product_ndc |
| ndc11 | package | 11673070838 | derived:openfda.package_ndc |
| spl id | 4b1e3edc-e0f6-1af3-e063-6394a90a4a1b | id | |
| spl set id | a8e52a22-7c30-40c0-8f78-523775743bfb | set_id | |
| unii | RHO26O1T9V | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings for this product
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse Reaction Dist. by Target Corp., Mpls., MN 55403 Made in U.S.A. with U.S. and Foreign components TM & ©2024 Target Brands, Inc.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.