MYDERM MEDICAL 5 LIDOCAINE NUMBING ROLL-ON- lidocaine stick 
Inspec Solutions

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MyDerm 5% Numbing Roll-On (IS0340)

Active Ingredient

Lidocaine 5%

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

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

For external use only.

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.

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

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

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

For external use only

MyDerm 5 Lidocaine

MYDERM MEDICAL 5 LIDOCAINE NUMBING ROLL-ON 
lidocaine stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72667-072
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
DIMETHICONE 100 (UNII: RO266O364U)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
ALCOHOL (UNII: 3K9958V90M)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
STEARETH-21 (UNII: 53J3F32P58)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72667-072-0189 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01503/06/2024
Labeler - Inspec Solutions (081030372)
Establishment
NameAddressID/FEIBusiness Operations
Inspec Solutions081030372manufacture(72667-072)

Revised: 6/2024
Document Id: 1ba1a028-c249-22c5-e063-6394a90ac2ae
Set id: 12ff170d-ce16-083a-e063-6394a90a4120
Version: 2
Effective Time: 20240624
 
Inspec Solutions