warnings
Warnings For external use only . Avoid contact with eyes, mucous membranes, damaged skin. Do not use with heating pads, avoid bandaging tightly. Stop use and ask doctor if : symptoms persist
SORE NO MORE
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
- SORE NO MORE
- Generic name
- MENTHOL CAMPHOR
- Manufacturer
- SOMBRA COSMETICS INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd
- SPL ID
- 4d785eb6-f915-92cc-e063-6294a90ad2f4
- Version
- 7
- Effective date
- 2026-03-20
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:32:31
| 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 | SORE NO MORE | openfda.brand_name | |
| generic name | MENTHOL CAMPHOR | openfda.generic_name | |
| manufacturer name | SOMBRA COSMETICS INC. | openfda.manufacturer_name | |
| ndc | package | 61577-2280-4 | openfda.package_ndc |
| ndc | package | 61577-2280-8 | openfda.package_ndc |
| ndc | package | 61577-2280-5 | openfda.package_ndc |
| ndc | package | 61577-2280-6 | openfda.package_ndc |
| ndc | package | 61577-2280-2 | openfda.package_ndc |
| ndc | product | 61577-2280 | openfda.product_ndc |
| ndc11 | package | 61577228002 | derived:openfda.package_ndc |
| ndc11 | package | 61577228008 | derived:openfda.package_ndc |
| ndc11 | package | 61577228005 | derived:openfda.package_ndc |
| ndc11 | package | 61577228006 | derived:openfda.package_ndc |
| ndc11 | package | 61577228004 | derived:openfda.package_ndc |
| rxcui | 630714 | openfda.rxcui | |
| rxcui | 1372559 | openfda.rxcui | |
| spl id | 4d785eb6-f915-92cc-e063-6294a90ad2f4 | id | |
| spl set id | 80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | 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.