Meijer Pain Lidocaine Plus Relieving Analgesic

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
Meijer Pain Lidocaine Plus Relieving Analgesic
Generic name
BENZYL ALCOHOL AND LIDOCAINE HYDROCHLORIDE
Manufacturer
Meijer Distribution, Inc
Product type
HUMAN OTC DRUG
SPL set ID
b7385140-3f63-4cbc-b557-de1d29d1ea36
SPL ID
115871ae-4a0c-4e20-9103-8327635ee318
Version
4
Effective date
2024-11-15
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:05:54
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Flammable Keep away from fire or flame Do not use If you ever had an allergic reaction to this product or any of its ingredients. When using this product avoid contact with the eyes do not use on damaged or broken skin do not bandage tightly do not use in large quantities, particularly over raw surfaces or blistered areas do not use with heating pads, medicated patches or heating devices use only as directed. Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days pain, swelling, blistering develops where product is used redness, rash, itching, irritation develops where product is used. If you are pregnant or nursing, seek the advice of a health professional before using. Keep out of reach of children . If swallowed, get medical help or contact a 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.