warnings
Warnings <Sore throat warnings: if sore throat is severe, persist for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious.>
Halls Sugar Free Honey Lemon
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 Sugar Free Honey Lemon
- Generic name
- MENTHOL
- Manufacturer
- Mondelez Global LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2b19fdd2-8088-47f2-be20-f220a6b825fc
- SPL ID
- 407f2207-a647-78ee-e063-6394a90add7e
- Version
- 10
- Effective date
- 2025-10-06
- Source export date
- 2026-10-27
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:27:10
| 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 Sugar Free Honey Lemon | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Mondelez Global LLC | openfda.manufacturer_name | |
| ndc | package | 12546-642-25 | openfda.package_ndc |
| ndc | package | 12546-642-30 | openfda.package_ndc |
| ndc | package | 12546-642-02 | openfda.package_ndc |
| ndc | package | 12546-642-70 | openfda.package_ndc |
| ndc | package | 12546-642-79 | openfda.package_ndc |
| ndc | product | 12546-642 | openfda.product_ndc |
| ndc11 | package | 12546064225 | derived:openfda.package_ndc |
| ndc11 | package | 12546064270 | derived:openfda.package_ndc |
| ndc11 | package | 12546064202 | derived:openfda.package_ndc |
| ndc11 | package | 12546064279 | derived:openfda.package_ndc |
| ndc11 | package | 12546064230 | derived:openfda.package_ndc |
| rxcui | 897006 | openfda.rxcui | |
| rxcui | 359751 | openfda.rxcui | |
| spl id | 407f2207-a647-78ee-e063-6394a90add7e | id | |
| spl set id | 2b19fdd2-8088-47f2-be20-f220a6b825fc | 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.