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
26e3a678-b28f-588b-e063-6394a90ac025
SPL ID
29880f16-792e-934d-e063-6294a90a5f34
Version
2
Effective date
2024-12-18
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:53:59

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.