MyDerm Pain Reliever Aloe Gel Lidocaine HCI 0.5%

Manufacturer
Inspec Solutions LLC.
Effective date
2025-04-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:39:29

Label at a glance#

ProductMyDerm
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Lidocaine ............. 0.5%

OTC - PURPOSE SECTION

Lidocaine 0.5% ............. Pain Reliever

INDICATIONS & USAGE SECTION

Temporary relief of pain and itching due to

- sunburn - minor burn - insect bites - minor cuts - scraps

WARNINGS SECTION

Warnings

For external use only

When using this product keep out of eyes

Rinse with warter to remove

OTC - STOP USE SECTION

Stop use and ask a doctor

system persist for more than 7 days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION

Direction

Adults and children 2 years and older: aooly to affected area not more that 3-4 times a day

Children under 2 years of age: consult a physician.

INACTIVE INGREDIENT SECTION


Inactive Ingredients: Aloe Barbadensis Leaf Extract, Carbomer, Diazolidinyl Urea, Disodium EDTA, Glycerin, Isopropyl Alcohol, Menthol, Polysorbate 80, Propylene Glycol, Triethanolamine, Water, Yellow 5.

OTC - DO NOT USE SECTION

Do not use in large quantities particularly over raw surfaces or blistered areas

OTC - QUESTIONS SECTION

Questions? 1-855-MYDERM1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MyDerm 0.5% label 20fl.ozMyDerm 0.5% label 20fl.oz

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72667-100MYDERM (LIDOCAINE) GEL [INSPEC SOLUTIONS LLC.]5Unmatched20250426_33857a07-7b3a-c639-e063-6294a90a4a24.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-10072667-100-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4af3b68f-0063-faa7-e063-6394a90afd4d33857a07-7b3a-c639-e063-6294a90a4a242026-02-16WarningsExact identifier
spl set id: 33857a07-7b3a-c639-e063-6294a90a4a24

Reported adverse events (FAERS/openFDA)#

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