warnings
Warnings
Pedia-Lax
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
- Pedia-Lax
- Generic name
- MAGNESIUM HYDROXIDE
- Manufacturer
- C.B. Fleet Company, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 975f24d8-218c-40f4-84a5-558acf34329d
- SPL ID
- ba6860a3-95dd-4ab8-8c1d-95aa836443f1
- Version
- 7
- Effective date
- 2024-04-11
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:36:57
| 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 | Pedia-Lax | openfda.brand_name | |
| generic name | MAGNESIUM HYDROXIDE | openfda.generic_name | |
| manufacturer name | C.B. Fleet Company, Inc. | openfda.manufacturer_name | |
| ndc | package | 0132-0655-01 | openfda.package_ndc |
| ndc | product | 0132-0655 | openfda.product_ndc |
| ndc11 | package | 00132065501 | derived:openfda.package_ndc |
| rxcui | 790436 | openfda.rxcui | |
| rxcui | 1088243 | openfda.rxcui | |
| spl id | ba6860a3-95dd-4ab8-8c1d-95aa836443f1 | id | |
| spl set id | 975f24d8-218c-40f4-84a5-558acf34329d | set_id | |
| unii | NBZ3QY004S | 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.