warnings
Warnings
Medique Alcalak
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
- Medique Alcalak
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- Unifirst First Aid Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 60703e3d-52b1-49c4-b4e2-59d96fa09a78
- SPL ID
- 3e4be5ad-5b19-b8da-e063-6394a90a50d6
- Version
- 17
- Effective date
- 2025-09-08
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:29:06
| 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 | M001 | openfda.application_number | |
| brand name | Medi-First Antacid | openfda.brand_name | |
| brand name | Medique Alcalak | openfda.brand_name | |
| brand name | Medi-First Plus Antacid | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | Unifirst First Aid Corporation | openfda.manufacturer_name | |
| ndc | package | 47682-201-33 | openfda.package_ndc |
| ndc | package | 47682-920-48 | openfda.package_ndc |
| ndc | package | 47682-820-50 | openfda.package_ndc |
| ndc | package | 47682-820-48 | openfda.package_ndc |
| ndc | package | 47682-820-13 | openfda.package_ndc |
| ndc | package | 47682-201-99 | openfda.package_ndc |
| ndc | package | 47682-820-33 | openfda.package_ndc |
| ndc | package | 47682-820-99 | openfda.package_ndc |
| ndc | package | 47682-201-13 | openfda.package_ndc |
| ndc | package | 47682-201-64 | openfda.package_ndc |
| ndc | package | 47682-920-33 | openfda.package_ndc |
| ndc | package | 47682-201-47 | openfda.package_ndc |
| ndc | package | 47682-201-69 | openfda.package_ndc |
| ndc | product | 47682-820 | openfda.product_ndc |
| ndc | product | 47682-920 | openfda.product_ndc |
| ndc | product | 47682-201 | openfda.product_ndc |
| ndc11 | package | 47682082099 | derived:openfda.package_ndc |
| ndc11 | package | 47682082050 | derived:openfda.package_ndc |
| ndc11 | package | 47682020199 | derived:openfda.package_ndc |
| ndc11 | package | 47682082033 | derived:openfda.package_ndc |
| ndc11 | package | 47682092048 | derived:openfda.package_ndc |
| ndc11 | package | 47682082048 | derived:openfda.package_ndc |
| ndc11 | package | 47682020169 | derived:openfda.package_ndc |
| ndc11 | package | 47682092033 | derived:openfda.package_ndc |
| ndc11 | package | 47682020113 | derived:openfda.package_ndc |
| ndc11 | package | 47682020147 | derived:openfda.package_ndc |
| ndc11 | package | 47682020133 | derived:openfda.package_ndc |
| ndc11 | package | 47682082013 | derived:openfda.package_ndc |
| ndc11 | package | 47682020164 | derived:openfda.package_ndc |
| rxcui | 313884 | openfda.rxcui | |
| spl id | 3e4be5ad-5b19-b8da-e063-6394a90a50d6 | id | |
| spl set id | 60703e3d-52b1-49c4-b4e2-59d96fa09a78 | set_id | |
| unii | H0G9379FGK | 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.