warnings
Warnings < Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied by fever, headache, rash, swelling, or vomiting, consult a doctor promptly. These may be serious.>
Halls MENTHO-LYPTUS
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
- Halls MENTHO-LYPTUS
- Generic name
- MENTHOL
- Manufacturer
- Mondelez Global LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ff21cf0e-9811-4819-bdfc-17a950e9b114
- SPL ID
- 29a54d04-41f2-c4b7-e063-6294a90aaed7
- Version
- 10
- Effective date
- 2024-12-19
- 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 05:18:08
| 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 | M012 | openfda.application_number | |
| brand name | Halls MENTHO-LYPTUS | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Mondelez Global LLC | openfda.manufacturer_name | |
| ndc | package | 12546-112-96 | openfda.package_ndc |
| ndc | package | 12546-112-40 | openfda.package_ndc |
| ndc | package | 12546-112-30 | openfda.package_ndc |
| ndc | package | 12546-112-14 | openfda.package_ndc |
| ndc | package | 12546-112-89 | openfda.package_ndc |
| ndc | package | 12546-112-80 | openfda.package_ndc |
| ndc | product | 12546-112 | openfda.product_ndc |
| ndc11 | package | 12546011289 | derived:openfda.package_ndc |
| ndc11 | package | 12546011240 | derived:openfda.package_ndc |
| ndc11 | package | 12546011296 | derived:openfda.package_ndc |
| ndc11 | package | 12546011280 | derived:openfda.package_ndc |
| ndc11 | package | 12546011214 | derived:openfda.package_ndc |
| ndc11 | package | 12546011230 | derived:openfda.package_ndc |
| rxcui | 1250187 | openfda.rxcui | |
| rxcui | 485287 | openfda.rxcui | |
| spl id | 29a54d04-41f2-c4b7-e063-6294a90aaed7 | id | |
| spl set id | ff21cf0e-9811-4819-bdfc-17a950e9b114 | set_id | |
| unii | L7T10EIP3A | 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.