warnings
Warnings
QUALITY CHOICE Nausea Relief
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
- QUALITY CHOICE Nausea Relief
- Generic name
- SODIUM CITRATE DIHYDRATE
- Manufacturer
- QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d89e41c1-399a-4157-8d54-bfefe3b1c1cd
- SPL ID
- 401c4d5c-7ff4-3f9d-e063-6294a90ad71e
- Version
- 1
- Effective date
- 2025-10-01
- Source export date
- 2026-10-27
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:07:55
| 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 |
|---|---|---|---|
| brand name | QUALITY CHOICE Nausea Relief | openfda.brand_name | |
| generic name | SODIUM CITRATE DIHYDRATE | openfda.generic_name | |
| manufacturer name | QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) | openfda.manufacturer_name | |
| ndc | package | 83324-300-42 | openfda.package_ndc |
| ndc | product | 83324-300 | openfda.product_ndc |
| ndc11 | package | 83324030042 | derived:openfda.package_ndc |
| rxcui | 2002800 | openfda.rxcui | |
| spl id | 401c4d5c-7ff4-3f9d-e063-6294a90ad71e | id | |
| spl set id | d89e41c1-399a-4157-8d54-bfefe3b1c1cd | set_id | |
| unii | B22547B95K | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.