warnings
WARNINGS FOR EXTERNAL USE ONLY
LIQUIMAT ACNE TREATMENT AND COVER-UP
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
- LIQUIMAT ACNE TREATMENT AND COVER-UP
- Generic name
- SULFUR
- Manufacturer
- Summers Laboratories Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3cb843ad-f52a-4876-b844-d441af08b27f
- SPL ID
- 521b2d8d-115a-916b-e063-6294a90ac29e
- Version
- 11
- Effective date
- 2026-05-18
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:17:43
| 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 | LIQUIMAT ACNE TREATMENT AND COVER-UP | openfda.brand_name | |
| generic name | SULFUR | openfda.generic_name | |
| manufacturer name | Summers Laboratories Inc | openfda.manufacturer_name | |
| ndc | package | 11086-028-01 | openfda.package_ndc |
| ndc | product | 11086-028 | openfda.product_ndc |
| ndc11 | package | 11086002801 | derived:openfda.package_ndc |
| spl id | 521b2d8d-115a-916b-e063-6294a90ac29e | id | |
| spl set id | 3cb843ad-f52a-4876-b844-d441af08b27f | 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.