warnings
WARNING: If you are pregnant or nursing a baby, seek the advice of a healthcare professional before using this product.
Formula 303
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
- Formula 303
- Generic name
- VALERIAN ROOT, PASSIFLORA, MAGNESIUM CARBONATE
- Manufacturer
- Dee Cee Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 50d35250-36d4-24bf-e054-00144ff8d46c
- SPL ID
- 2b0c782e-6b9b-13fc-e063-6294a90a6ee8
- Version
- 5
- Effective date
- 2025-01-06
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:32
| 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 | Formula 303 | openfda.brand_name | |
| generic name | VALERIAN ROOT, PASSIFLORA, MAGNESIUM CARBONATE | openfda.generic_name | |
| manufacturer name | Dee Cee Laboratories | openfda.manufacturer_name | |
| ndc | package | 52301-303-45 | openfda.package_ndc |
| ndc | package | 52301-303-25 | openfda.package_ndc |
| ndc | package | 52301-303-60 | openfda.package_ndc |
| ndc | package | 52301-303-21 | openfda.package_ndc |
| ndc | package | 52301-303-12 | openfda.package_ndc |
| ndc | package | 52301-303-90 | openfda.package_ndc |
| ndc | package | 52301-303-30 | openfda.package_ndc |
| ndc | product | 52301-303 | openfda.product_ndc |
| ndc11 | package | 52301030360 | derived:openfda.package_ndc |
| ndc11 | package | 52301030390 | derived:openfda.package_ndc |
| ndc11 | package | 52301030321 | derived:openfda.package_ndc |
| ndc11 | package | 52301030312 | derived:openfda.package_ndc |
| ndc11 | package | 52301030330 | derived:openfda.package_ndc |
| ndc11 | package | 52301030345 | derived:openfda.package_ndc |
| ndc11 | package | 52301030325 | derived:openfda.package_ndc |
| spl id | 2b0c782e-6b9b-13fc-e063-6294a90a6ee8 | id | |
| spl set id | 50d35250-36d4-24bf-e054-00144ff8d46c | set_id | |
| unii | 0E53J927NA | openfda.unii | |
| unii | JWF5YAW3QW | openfda.unii | |
| unii | K8F3G29S6Z | 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.