warnings
Warnings: For external use only. Discontinue use if signs of irritation appear. If condition worsens consult a doctor. Do not use over deep, infected, or puncture wounds.
VERADEX-E
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
- VERADEX-E
- Generic name
- PETROLATUM AND LANOLIN
- Manufacturer
- ABBE Laboratories, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 00100102-c245-4b63-a4ff-794cacda6f17
- SPL ID
- 8a1f564e-f8eb-4ef1-b742-d83d6416f8d9
- Version
- 8
- Effective date
- 2026-01-24
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:14:25
| 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 | M016 | openfda.application_number | |
| brand name | VERADEX-E | openfda.brand_name | |
| generic name | PETROLATUM AND LANOLIN | openfda.generic_name | |
| manufacturer name | ABBE Laboratories, Inc. | openfda.manufacturer_name | |
| ndc | package | 68605-3700-4 | openfda.package_ndc |
| ndc | package | 68605-3700-3 | openfda.package_ndc |
| ndc | package | 68605-3700-6 | openfda.package_ndc |
| ndc | package | 68605-3700-2 | openfda.package_ndc |
| ndc | package | 68605-3700-5 | openfda.package_ndc |
| ndc | product | 68605-3700 | openfda.product_ndc |
| ndc11 | package | 68605370006 | derived:openfda.package_ndc |
| ndc11 | package | 68605370003 | derived:openfda.package_ndc |
| ndc11 | package | 68605370002 | derived:openfda.package_ndc |
| ndc11 | package | 68605370005 | derived:openfda.package_ndc |
| ndc11 | package | 68605370004 | derived:openfda.package_ndc |
| rxcui | 2618668 | openfda.rxcui | |
| spl id | 8a1f564e-f8eb-4ef1-b742-d83d6416f8d9 | id | |
| spl set id | 00100102-c245-4b63-a4ff-794cacda6f17 | set_id | |
| unii | 7EV65EAW6H | openfda.unii | |
| unii | 4T6H12BN9U | 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.