warnings
Warnings For external use only. Avoid contact with eyes. Do not take by mouth or place in nostrils.
Health Smart Vaporizing Chest Rub
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
- Health Smart Vaporizing Chest Rub
- Generic name
- MENTHOL AND CAMPHOR AND EUCALYPTUS OIL
- Manufacturer
- Jell Pharmaceuticals Pvt Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d80cad8d-da4c-049d-e053-2a95a90ac20e
- SPL ID
- 2987f3c3-6db5-5756-e063-6394a90a0a99
- Version
- 2
- Effective date
- 2024-12-18
- Source export date
- 2026-11-06
- 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/2026-11-06/7dfa569f2d8f065241260fd9a4886d0ef0a3120fd6ee31d6d07c234e689e8c91/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:24:54
| Harmonized routes |
|---|
| TOPICAL |
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 | Health Smart Vaporizing Chest Rub | openfda.brand_name | |
| generic name | MENTHOL AND CAMPHOR AND EUCALYPTUS OIL | openfda.generic_name | |
| manufacturer name | Jell Pharmaceuticals Pvt Ltd. | openfda.manufacturer_name | |
| ndc | package | 30400-702-02 | openfda.package_ndc |
| ndc | package | 30400-702-03 | openfda.package_ndc |
| ndc | package | 30400-702-01 | openfda.package_ndc |
| ndc | product | 30400-702 | openfda.product_ndc |
| ndc11 | package | 30400070202 | derived:openfda.package_ndc |
| ndc11 | package | 30400070203 | derived:openfda.package_ndc |
| ndc11 | package | 30400070201 | derived:openfda.package_ndc |
| rxcui | 1042788 | openfda.rxcui | |
| spl id | 2987f3c3-6db5-5756-e063-6394a90a0a99 | id | |
| spl set id | d80cad8d-da4c-049d-e053-2a95a90ac20e | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii | |
| unii | 2R04ONI662 | 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.