Dr. Scholls Blister Pain Relief Complete

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
Dr. Scholls Blister Pain Relief Complete
Generic name
LIDOCAINE
Manufacturer
Scholl's Wellness Company LLC
Product type
HUMAN OTC DRUG
SPL set ID
d860b339-48a0-405c-a67d-f7e7a31f6351
SPL ID
29881241-9409-5681-e063-6394a90a22d3
Version
2
Effective date
2024-12-18
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:56:24

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Avoid contact with eyes If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Do not use More than one patch on your body at a time If you have had an allergic reaction to lidocaine or other local anesthetics Do not use in large quantities, particularly over raw surfaces or blistered areas 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 Stop use and ask a doctor if condition worsens severe burning sensation, redness, rash or irritation develops symptoms persist for more than 7 days or clear up and occur again within a few days you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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