warnings
Warnings For external use only Avoid contact with eyes and mucous membranes
Aulief Topical Pain Reliever
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
- Aulief Topical Pain Reliever
- Generic name
- MENTHOL AND CAMOHOR
- Manufacturer
- China-Gel, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 8647dcc3-1dbc-1093-e053-2991aa0a1ab9
- SPL ID
- 42c89af1-c7d8-0ee3-e063-6394a90a3aef
- Version
- 4
- Effective date
- 2025-11-04
- Source export date
- 2026-11-06
- 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/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:47:26
| 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 | Aulief Topical Pain Reliever | openfda.brand_name | |
| generic name | MENTHOL AND CAMOHOR | openfda.generic_name | |
| manufacturer name | China-Gel, LLC | openfda.manufacturer_name | |
| ndc | package | 76305-302-03 | openfda.package_ndc |
| ndc | package | 76305-302-01 | openfda.package_ndc |
| ndc | package | 76305-302-02 | openfda.package_ndc |
| ndc | product | 76305-302 | openfda.product_ndc |
| ndc11 | package | 76305030202 | derived:openfda.package_ndc |
| ndc11 | package | 76305030203 | derived:openfda.package_ndc |
| ndc11 | package | 76305030201 | derived:openfda.package_ndc |
| rxcui | 2168358 | openfda.rxcui | |
| rxcui | 1312283 | openfda.rxcui | |
| spl id | 42c89af1-c7d8-0ee3-e063-6394a90a3aef | id | |
| spl set id | 8647dcc3-1dbc-1093-e053-2991aa0a1ab9 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | N20HL7Q941 | 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.