AIPATCH NUMBING PAIN 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 (canonical bytes are SHA-256 checked before publication)

Brand name
AIPATCH NUMBING PAIN RELIEF
Generic name
LIDOCAINE
Manufacturer
Active Intelligence, LLC
Product type
HUMAN OTC DRUG
SPL set ID
56f27540-9b2a-4266-9e15-a5b2d738c7a1
SPL ID
c8c5154c-e183-4a78-bb6c-582602e0973f
Version
1
Effective date
2025-07-25
Source export date
2026-08-01
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:05:01
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings for external use only When using this product • use only as directed. Read and follow all directions and warnings on this carton • do not bandage tightly • avoid contact with eyes and mucous membranes • do not use at the same time as other topical analgesics • do not remove when wet or directly after shower, allow to dry and then slowly remove Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days • you experience signs of skin injury, such as pain, swelling or blistering where the patch was applied • If pregnant or breast-feeding, ask a health professional before use • If swallowed, get medical help or contact a Poison Control Center right away