warnings
Warnings For external use only; avoid contact with eyes
cough suppressant and topical analgesic
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
- cough suppressant and topical analgesic
- Generic name
- CAMPHOR, EUCALYPTUS OIL, MENTHOL
- Manufacturer
- Target Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- df21d9d6-36a9-49cf-a29c-c4a573899bd5
- SPL ID
- 4b1e7206-1f3d-b750-e063-6394a90a36dc
- Version
- 17
- Effective date
- 2026-02-18
- 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/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:03:19
| 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 | cough suppressant and topical analgesic | openfda.brand_name | |
| generic name | CAMPHOR, EUCALYPTUS OIL, MENTHOL | openfda.generic_name | |
| manufacturer name | Target Corporation | openfda.manufacturer_name | |
| ndc | package | 11673-667-02 | openfda.package_ndc |
| ndc | product | 11673-667 | openfda.product_ndc |
| ndc11 | package | 11673066702 | derived:openfda.package_ndc |
| rxcui | 727137 | openfda.rxcui | |
| spl id | 4b1e7206-1f3d-b750-e063-6394a90a36dc | id | |
| spl set id | df21d9d6-36a9-49cf-a29c-c4a573899bd5 | 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.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
adverse reactions section FAILURE TO FOLLOW THESE WARNINGS COULD RESULT IN SERIOUS CONSEQUENCES *This product is not manufactured or distributed by Procter & Gamble, distributor of Vicks ® VapoRub ® Dist. By Target Corp. Mpls., MN 55403
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.