Numb Master

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
Numb Master
Generic name
LIDOCAINE
Manufacturer
Clinical Resolution Laboratory, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
0921c824-a8a9-4707-a480-c750192983f5
SPL ID
4a6d5776-54cb-449a-e063-6394a90a00ff
Version
4
Effective date
2026-02-09
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 05:35:18
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) Do not use this product if pregnant or breastfeeding, ask a health professional before use. in case of accidental overdose, get medical help or contact the Poison Control Center immediately. tamper evident "Do not use this product" if seal is broken or missing. When using this product do not exceed the recommended daily dosage unless directed by a doctor. certain persons can develop allergic reactions to ingredients in this product. do not put this product into the rectum by using finger or any medical device or applicator. Stop use and ask a doctor if the symptom being treated does not subside, or if redness, irritation, swelling, pain, or other symptoms develop or increase. Keep out of reach of children In case of accidental ingestion, seek medical attention immediately.

Reported adverse events (FAERS/openFDA)#

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