warnings
Warnings For external use only. Do not use in the eyes. In case of contact, immediately flush eyes with water.
Maxim FDF
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
- Maxim FDF
- Generic name
- CHLOROXYLENOL
- Manufacturer
- Midlab Incorporated
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 83d26ca6-b075-edab-e053-2991aa0add3f
- SPL ID
- 3b00d424-86a6-00f7-e063-6294a90a980c
- Version
- 9
- Effective date
- 2025-07-28
- 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 06:37:40
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Maxim FDF | openfda.brand_name | |
| generic name | CHLOROXYLENOL | openfda.generic_name | |
| manufacturer name | Midlab Incorporated | openfda.manufacturer_name | |
| ndc | package | 70542-201-41 | openfda.package_ndc |
| ndc | package | 70542-201-55 | openfda.package_ndc |
| ndc | product | 70542-201 | openfda.product_ndc |
| ndc11 | package | 70542020141 | derived:openfda.package_ndc |
| ndc11 | package | 70542020155 | derived:openfda.package_ndc |
| rxcui | 1941461 | openfda.rxcui | |
| spl id | 3b00d424-86a6-00f7-e063-6294a90a980c | id | |
| spl set id | 83d26ca6-b075-edab-e053-2991aa0add3f | set_id | |
| unii | 0F32U78V2Q | 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.