Nupharmisto NumbMD LIDOCAINE cream anorectal (hemorrhoidal)

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
Nupharmisto NumbMD LIDOCAINE cream anorectal (hemorrhoidal)
Generic name
LIDOCAINE CREAM ANORECTAL
Manufacturer
EveryMarket Inc
Product type
HUMAN OTC DRUG
SPL set ID
483d81a3-7493-3391-e063-6394a90a2e3d
SPL ID
58da9e72-b7ca-6d6e-e063-6394a90a9b4f
Version
2
Effective date
2026-08-12
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:46:27
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

For external use only If condition worsens or does not improve within 7 days,consult a doctor. Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding,consult a doctor promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator.

Reported adverse events (FAERS/openFDA)#

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