FDA.reportPublic FDA data

MyDerm Medical 5 Lidocaine Numbing Roll-On

Manufacturer
Inspec Solutions
Effective date
2024-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:59:53

Label at a glance#

ProductMyDerm Medical 5 Lidocaine Numbing Roll-On
Active ingredientLIDOCAINE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Lidocaine 5%

OTC - WHEN USING SECTION

When using this product avoid conatct with the eyes or muccous membranes.

OTC - PURPOSE SECTION

Lidocaine 5% ------------------------------------------------------------Local Anesthetic

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use and ask doctor if condition worsens, or symtoms persist for more than 7 days,or clear up and reoccur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer

Aloe Vera Barbadensis Leaft Juice

Inactive ingredients

2-animo-2methyl-1propanol

2-Methylamino-2-methyl-1-propanol

Cetearyl Alcohol

Citric Acid

Dimethicone

Disodium EDTA

Ethanol

Ethyhexylglycerin

Glyceril Stearate

Phenoxyethanol

Potassium Sorbate

Silicone Gel

Sodium Benzoate

Steareth-21

Water

DOSAGE & ADMINISTRATION SECTION

Apply to affected area not more than 3 to 4 times daily

INDICATIONS & USAGE SECTION

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MyDerm 5 LidocaineMyDerm 5 Lidocaine

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-07272667-072-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOMETHYLPROPANOLLU49E6626QIACT
DIMETHICONE 100RO266O364UIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ALOE VERA LEAFZY81Z83H0XIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
ALCOHOL3K9958V90MIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CITRIC ACID ACETATEDSO12WL7AUIACT
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
SODIUM BENZOATEOJ245FE5EUIACT
LIDOCAINE98PI200987ACTIB
CETOSTEARYL ALCOHOL2DMT128M1SIACT
STEARETH-2153J3F32P58IACT

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
3531319c-1189-7216-e063-6294a90ac8ff12ff170d-ce16-083a-e063-6394a90a41202025-05-15WarningsExact identifier
spl set id: 12ff170d-ce16-083a-e063-6394a90a4120

Reported adverse events (FAERS/openFDA)#

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