ZHENG GU SHUI
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
- ZHENG GU SHUI
- Generic name
- CAMPHOR, MENTHOL
- Manufacturer
- GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 17552943-4f11-42d6-ad41-fbc53f2bbd9a
- SPL ID
- 436cb650-b183-07c4-e063-6294a90ae29d
- Version
- 5
- Effective date
- 2025-11-12
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:05:12
| Harmonized routes |
|---|
| PERCUTANEOUS, TRANSDERMAL |
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 | ZHENG GU SHUI | openfda.brand_name | |
| generic name | CAMPHOR, MENTHOL | openfda.generic_name | |
| manufacturer name | GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD | openfda.manufacturer_name | |
| ndc | package | 59321-055-05 | openfda.package_ndc |
| ndc | package | 59321-055-02 | openfda.package_ndc |
| ndc | package | 59321-055-03 | openfda.package_ndc |
| ndc | package | 59321-055-01 | openfda.package_ndc |
| ndc | package | 59321-055-04 | openfda.package_ndc |
| ndc | product | 59321-055 | openfda.product_ndc |
| ndc11 | package | 59321005504 | derived:openfda.package_ndc |
| ndc11 | package | 59321005505 | derived:openfda.package_ndc |
| ndc11 | package | 59321005502 | derived:openfda.package_ndc |
| ndc11 | package | 59321005503 | derived:openfda.package_ndc |
| ndc11 | package | 59321005501 | derived:openfda.package_ndc |
| rxcui | 1366315 | openfda.rxcui | |
| spl id | 436cb650-b183-07c4-e063-6294a90ae29d | id | |
| spl set id | 17552943-4f11-42d6-ad41-fbc53f2bbd9a | 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.
Warnings For external use only Flammable Keep away from fire or flame
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Report any unexpected side effects from the use of this product to the FDA MedWatch Program.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.