warnings
Warnings For External Use Only.
Katinko Pain And Itch Relieving
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
- Katinko Pain And Itch Relieving
- Generic name
- CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
- Manufacturer
- Greenstone Pharmaceutical Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- fe907fa4-4a01-4974-b71f-9cd980b4eaa2
- SPL ID
- 0c0d4eac-3530-250d-e063-6294a90aad14
- Version
- 8
- Effective date
- 2023-12-08
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:35:10
| 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 | M017 | openfda.application_number | |
| brand name | Katinko Pain And Itch Relieving | openfda.brand_name | |
| generic name | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE | openfda.generic_name | |
| manufacturer name | Greenstone Pharmaceutical Inc. | openfda.manufacturer_name | |
| ndc | package | 52241-100-10 | openfda.package_ndc |
| ndc | package | 52241-100-03 | openfda.package_ndc |
| ndc | package | 52241-100-30 | openfda.package_ndc |
| ndc | product | 52241-100 | openfda.product_ndc |
| ndc11 | package | 52241010030 | derived:openfda.package_ndc |
| ndc11 | package | 52241010003 | derived:openfda.package_ndc |
| ndc11 | package | 52241010010 | derived:openfda.package_ndc |
| rxcui | 1542816 | openfda.rxcui | |
| rxcui | 1542818 | openfda.rxcui | |
| spl id | 0c0d4eac-3530-250d-e063-6294a90aad14 | id | |
| spl set id | fe907fa4-4a01-4974-b71f-9cd980b4eaa2 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii | |
| unii | LAV5U5022Y | 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
Other Information This product make provoke allergic reaction in some individuals. Test on small area before use.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.