warnings
Warnings For external use only
Asper Flex
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
- Asper Flex
- Generic name
- LIDOCAINE
- Manufacturer
- Akron Pharma Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 06ddae64-cda7-4eb9-872f-5182c83cb00c
- SPL ID
- 3f2cef5f-9c8b-a1af-e063-6294a90a2e74
- Version
- 4
- Effective date
- 2025-09-19
- Source export date
- 2026-09-28
- 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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:54:23
| 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 | M017 | openfda.application_number | |
| brand name | Asper Flex | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Akron Pharma Inc. | openfda.manufacturer_name | |
| ndc | package | 71399-0049-3 | openfda.package_ndc |
| ndc | package | 71399-0049-2 | openfda.package_ndc |
| ndc | package | 71399-0049-1 | openfda.package_ndc |
| ndc | product | 71399-0049 | openfda.product_ndc |
| ndc11 | package | 71399004901 | derived:openfda.package_ndc |
| ndc11 | package | 71399004903 | derived:openfda.package_ndc |
| ndc11 | package | 71399004902 | derived:openfda.package_ndc |
| rxcui | 1421893 | openfda.rxcui | |
| spl id | 3f2cef5f-9c8b-a1af-e063-6294a90a2e74 | id | |
| spl set id | 06ddae64-cda7-4eb9-872f-5182c83cb00c | set_id | |
| unii | 98PI200987 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings
For external use only Do not use in or near the eyes in large quantities, particularly over raw or blistered areas Stop use and ask a doctor if allergic reaction occurs condition worsens or does not improve within 7 days symptoms clear up and return within a few days redness, irritation, swelling, pain or other symptoms begin or increase Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.