Honest Med Lidocaine Lavender Roll-on

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
Honest Med Lidocaine Lavender Roll-on
Generic name
LIDOCAINE HCL
Manufacturer
Proper Buys LLC
Product type
HUMAN OTC DRUG
SPL set ID
2dcd40a9-3fdd-a71e-e063-6294a90a704f
SPL ID
47060238-11e7-f720-e063-6294a90ac785
Version
2
Effective date
2025-12-28
Source export date
2026-11-06
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:52:57
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 On large areas of the body or on cut, irritated or swollen skin ■ on puncture wounds ■for more than one week without consulting a doctor When using this product ■use only as directed. Read and follow all directions and warnings on this carton ■do not allow contact with the eyes and mucous membranes ■ do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use ■do not use at the same time as other topical analgesics Stop use and ask a doctor if ■ condition worsens ■ redness is present ■irritation develops ■symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breastfeeding ask a health professional before use Keep out of reach of children and pets If swallowed, get medical help or contact Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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