warnings
WARNINGS FOR EXTERNAL USE ONLY
EradiKate ACNE TREATMENT
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
- EradiKate ACNE TREATMENT
- Generic name
- SULFUR
- Manufacturer
- Rare Beauty Brands Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 44ebacf3-52c1-4896-e063-6394a90ac447
- SPL ID
- 44eba48d-5fc8-38ea-e063-6394a90ad2e9
- Version
- 9
- Effective date
- 2025-12-01
- Source export date
- 2026-09-28
- 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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:52
| 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 | EradiKate ACNE TREATMENT | openfda.brand_name | |
| generic name | SULFUR | openfda.generic_name | |
| manufacturer name | Rare Beauty Brands Inc | openfda.manufacturer_name | |
| ndc | package | 72204-901-02 | openfda.package_ndc |
| ndc | package | 72204-901-01 | openfda.package_ndc |
| ndc | product | 72204-901 | openfda.product_ndc |
| ndc11 | package | 72204090101 | derived:openfda.package_ndc |
| ndc11 | package | 72204090102 | derived:openfda.package_ndc |
| rxcui | 198869 | openfda.rxcui | |
| spl id | 44eba48d-5fc8-38ea-e063-6394a90ad2e9 | id | |
| spl set id | 44ebacf3-52c1-4896-e063-6394a90ac447 | set_id | |
| 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.