FDA label 7ba331f7-2b5d-431d-bef4-8a427c564fad

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)

SPL set ID
09299ae8-ab15-4291-ab51-f476c9e2f0fd
SPL ID
7ba331f7-2b5d-431d-bef4-8a427c564fad
Version
4
Effective date
2019-02-12
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 06:09:39

Warnings cross-check#

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Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings: • For external use only. Use only as directed or by a health professional. • Do not use: On wounds, cuts, damaged or infected skin. - On eyes, mouth, genitals, or any other mucus membranes. • Stop and consult your physician if pregnant or if pain worsens • Allergy Alert: if you are allergic to any ingredients of this product or chili peppers contact a doctor before use.

warnings and cautions

WARNINGS: 1. Do not use: • On wounds, cuts, damaged or infected skin • On eyes, mouth, genitals, or other mucous membranes 2. Consult physician for children under 12 years of age 3. Stop and consult your prescriber if pain worsens 4. DISCONTINUE USE AT LEAST 1 HOURS BEFORE A BATH OR SHOWER AND DO NOT USE IMMEDIATELY AFTER A BATH OR SHOWER Call your healthcare provider right away if you get any of the following warning signs or any other unusual symptoms that concern you: • Shortness of breath • Swelling or numbness of the tongue or throat • Severe headache or vomiting • Dizziness or faintness • Changes in vision or speech This is not a complete list of the possible side effects. For more information, talk with your doctor or pharmacist. You may report side effects to FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTIONS: The most common adverse reactions are application site reactions, including dermatitis, itching or scaling. These tend to be dose-limiting and diminish with time. Serious adverse experiences following the administration of MenCaps Patch ® are similar in nature to those observed in other amide anesthetic-containing agents. These adverse experiences are, in general, dose-related and may result from high plasma levels caused by excessive dosage, rapid absorption, or may result from hypersensitivity, idiosyncrasy, or a diminished tolerance on the part of the patient. Serious adverse experiences are generally systemic in nature.

Reported adverse events (FAERS/openFDA)#

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