warnings
Warnings For external use only . When using this product do not use in or near eyes. Stop use and ask a doctor if symptoms last more than 3 days, symptoms worsen, or symptoms clear up and occur again within a few days.
Terrasil Balanitis Relief
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
- Terrasil Balanitis Relief
- Generic name
- SULFUR, SYMPHYTUM OFFICINALE (COMFREY)
- Manufacturer
- Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 16c243e0-dec4-4643-949f-48dfd6bc5c08
- SPL ID
- 2763f0a0-abfe-19d4-e063-6394a90a1a7e
- Version
- 4
- Effective date
- 2024-11-20
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:09:22
| 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 | Terrasil Balanitis Relief | openfda.brand_name | |
| generic name | SULFUR, SYMPHYTUM OFFICINALE (COMFREY) | openfda.generic_name | |
| manufacturer name | Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions | openfda.manufacturer_name | |
| ndc | package | 24909-119-15 | openfda.package_ndc |
| ndc | package | 24909-119-28 | openfda.package_ndc |
| ndc | package | 24909-119-44 | openfda.package_ndc |
| ndc | package | 24909-119-50 | openfda.package_ndc |
| ndc | package | 24909-119-14 | openfda.package_ndc |
| ndc | product | 24909-119 | openfda.product_ndc |
| ndc11 | package | 24909011914 | derived:openfda.package_ndc |
| ndc11 | package | 24909011915 | derived:openfda.package_ndc |
| ndc11 | package | 24909011928 | derived:openfda.package_ndc |
| ndc11 | package | 24909011950 | derived:openfda.package_ndc |
| ndc11 | package | 24909011944 | derived:openfda.package_ndc |
| spl id | 2763f0a0-abfe-19d4-e063-6394a90a1a7e | id | |
| spl set id | 16c243e0-dec4-4643-949f-48dfd6bc5c08 | set_id | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | H8FJJ6KX5Y | 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.