warnings
Warnings For external use only; avoid contact with eyes.
Vicks VapoRub
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
- Vicks VapoRub
- Generic name
- CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL
- Manufacturer
- Procter & Gamble Manufactura S de RL de CV
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 699691ae-d2a1-a8bb-e053-2991aa0acfea
- SPL ID
- 401d5a24-e364-cb12-e063-6394a90aae60
- Version
- 12
- Effective date
- 2025-10-01
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:52
| 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 | Vicks VapoRub | openfda.brand_name | |
| generic name | CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL | openfda.generic_name | |
| manufacturer name | Procter & Gamble Manufactura S de RL de CV | openfda.manufacturer_name | |
| ndc | package | 58933-544-45 | openfda.package_ndc |
| ndc | package | 58933-544-03 | openfda.package_ndc |
| ndc | package | 58933-544-06 | openfda.package_ndc |
| ndc | package | 58933-544-12 | openfda.package_ndc |
| ndc | package | 58933-544-02 | openfda.package_ndc |
| ndc | package | 58933-544-01 | openfda.package_ndc |
| ndc | package | 58933-544-15 | openfda.package_ndc |
| ndc | product | 58933-544 | openfda.product_ndc |
| ndc11 | package | 58933054445 | derived:openfda.package_ndc |
| ndc11 | package | 58933054415 | derived:openfda.package_ndc |
| ndc11 | package | 58933054403 | derived:openfda.package_ndc |
| ndc11 | package | 58933054402 | derived:openfda.package_ndc |
| ndc11 | package | 58933054406 | derived:openfda.package_ndc |
| ndc11 | package | 58933054412 | derived:openfda.package_ndc |
| ndc11 | package | 58933054401 | derived:openfda.package_ndc |
| rxcui | 727137 | openfda.rxcui | |
| spl id | 401d5a24-e364-cb12-e063-6394a90aae60 | id | |
| spl set id | 699691ae-d2a1-a8bb-e053-2991aa0acfea | 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.