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
- 2026-11-06
- 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/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:16:27
| 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.