INSTA RELIEF DM- lidocaine hydrochloride, menthol cream 
DM LAB CORP

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INSTA-RELIEF DM

DRUG FACTS

ACTIVE INGREDIENTS

Lidocaine HCL 4.00%

Menthol 1.00%

Topical Anesthetic

INDICATIONS:

For the temporary relief of pain and itching assoicated with minor burns sunburn, minor cuts, scrapes, insect bites or minor skin irritations.

WARNINGS

Keep out of reach of children.

If swallowed, consult physician.

Do not apply

  • to wounds or damaged skin.
  • Do not bandage tightly.

If pregnant or breast feeding,

contact physician

DIRECTIONS:

Additional Information:

Store at room temperature.

OTHER INGREDIENTS:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Benzyl Alchol, Caprylic/Capric Triglyceride, Carbomer, Cetearyl Alcohol, Cetereth-20, Cetyl Alcohol, Citrus Aurantifolia (Orange) Oil, Daucus Carota Sativa (Carrot) Extract, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, 1-Arginine, Lavandula Angustifolia (Lavender) Oil, Lecithin, Methylsulfonylmethane (MSM), Phenoxyethanol, Potassium Hydroxide

Package Labeling:

Label

INSTA RELIEF DM 
lidocaine hydrochloride, menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72465-600
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
LIME OIL (UNII: UZH29XGA8G)  
CARROT (UNII: L56Z1JK48B)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72465-600-00118 mL in 1 JAR; Type 0: Not a Combination Product07/05/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/05/2018
Labeler - DM LAB CORP (099396086)

Revised: 11/2023
Document Id: 097478f1-9b6a-b749-e063-6394a90a9977
Set id: 6ef66fb9-9f49-409d-9503-175c7555ee9e
Version: 2
Effective Time: 20231105
 
DM LAB CORP