Dr.Johnes Lidocaine 4% Topical Analgesic Cream

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
Dr.Johnes Lidocaine 4% Topical Analgesic Cream
Generic name
LIDOCAINE HCL,MENTHOL
Manufacturer
Dr.Johnes LLC
Product type
HUMAN OTC DRUG
SPL set ID
6144708d-4b0f-4f0d-88e3-6925ba2d004d
SPL ID
45f8588a-99a1-443e-b435-df1fef7f08a4
Version
2
Effective date
2026-06-29
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:15
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only Do not use: on open wounds or damaged skin. in large quantities, especially over raw surfaces. if allergic to lidocaine, menthol, or any ingredients in this product. When using this product: Avoid contact with eyes and mucous membranes. Do not bandage tightly or use heating pad. Discontinue use if excessive irritation occurs. Stop use and ask a doctor if: condition worsens. Symptoms persist for more than 7 days. Severe burning, redness, or irritation develops. If pregnant or breast-feeding Ask a health professional before use Keep out of reach of children. If swallowed, get medical help or contact Poison Control immediately.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.