Rite Aid Pain Relieving 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
Rite Aid Pain Relieving Roll-On
Generic name
LIDOCAINE HCL
Manufacturer
Rite Aid Corporation
Product type
HUMAN OTC DRUG
SPL set ID
1406590c-667c-84eb-e063-6294a90a5052
SPL ID
1fcd7134-c44b-1b6a-e063-6394a90ad80e
Version
2
Effective date
2024-08-16
Source export date
2026-10-30
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:37:41
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warning 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 Flammable Keep away from fire or flame Store at room temperature If pregnant or breast feeding, ask a health professional before use Keep out if 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.