warnings
Warnings For external use only
Adult Acnomel
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
- Adult Acnomel
- Generic name
- RESORCINOL, SULFUR
- Manufacturer
- NUMARK BRANDS, INC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 90f80e35-095d-88f9-8ea3-0fd54f1e916c
- SPL ID
- c0b864bb-735e-4510-b30f-9eae4f5c8b03
- Version
- 12
- Effective date
- 2025-12-03
- Source export date
- 2026-09-28
- 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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:47
| 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 | M006 | openfda.application_number | |
| brand name | Adult Acnomel | openfda.brand_name | |
| generic name | RESORCINOL, SULFUR | openfda.generic_name | |
| manufacturer name | NUMARK BRANDS, INC | openfda.manufacturer_name | |
| ndc | package | 69846-911-61 | openfda.package_ndc |
| ndc | product | 69846-911 | openfda.product_ndc |
| ndc11 | package | 69846091161 | derived:openfda.package_ndc |
| rxcui | 209990 | openfda.rxcui | |
| rxcui | 312793 | openfda.rxcui | |
| spl id | c0b864bb-735e-4510-b30f-9eae4f5c8b03 | id | |
| spl set id | 90f80e35-095d-88f9-8ea3-0fd54f1e916c | set_id | |
| unii | YUL4LO94HK | openfda.unii | |
| unii | 70FD1KFU70 | 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.