warnings
Warnings • For external use only • Do not use in eyes • Ask a doctor before use if you have deep puncture wounds or serious burns •
Ichthammol 20%
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
- Ichthammol 20%
- Generic name
- ICHTHAMMOL
- Manufacturer
- Chain Drug Marketing Association, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1cc52246-bec4-2d44-e063-6394a90a625b
- SPL ID
- 1cc52258-5150-de0c-e063-6294a90ac035
- Version
- 1
- Effective date
- 2024-07-08
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:24:26
| 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 |
|---|---|---|---|
| brand name | Ichthammol 20% | openfda.brand_name | |
| generic name | ICHTHAMMOL | openfda.generic_name | |
| manufacturer name | Chain Drug Marketing Association, Inc. | openfda.manufacturer_name | |
| ndc | package | 83324-048-01 | openfda.package_ndc |
| ndc | product | 83324-048 | openfda.product_ndc |
| ndc11 | package | 83324004801 | derived:openfda.package_ndc |
| spl id | 1cc52258-5150-de0c-e063-6294a90ac035 | id | |
| spl set id | 1cc52246-bec4-2d44-e063-6394a90a625b | set_id | |
| unii | NQ14646378 | 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.