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Solmara

Medically reviewed on July 21, 2017.

Dosage form: patch
Ingredients: Menthol, Unspecified Form 5g, Lidocaine 4g
Labeler: Spring Hill Therapeutics LLC
NDC Code: 69833-011

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Solmara

Drug Facts

Active IngredientsPurpose
Menthol 5.00%Topical Analgesic
Lidocaine 4.00%Topical Anesthetic

Uses

For the temporary relief of minor aches and muscle pains associated with arthritis, simple backache, strains, muscle soreness and stiffness.

Warnings

Only for external use. Use only as directed or by a health professional.

Do not use: on open wounds, cuts, damaged or infected skin as well as in the eyes, mouth, genitals, or any other mucous membranes.

Do not cover with bandage.

Keep out of the reach of children. Consult physician for children under 12.

Consult your physician: if pregnant or pain persists or worsens.

Directions

Adults and children 12 years and over. Apply patch to affected area 1 to 2 times daily or as directed.

Instruction for Use

Clean and dry the affected area

Open pouch and remove one patch

Remove any protective film and apply directly to affected area of pain

Wash hands with soap and water after applying patch

Reseal pouch containing unused patches after each use

Other Ingredients

Methacrylic acid, ethylhexylacrylate, bentonite, sodium stearate.

FOR QUESTIONS CALL 813-388-8735

PRINCIPAL DISPLAY PANEL - 15 Patch Carton

NDC 69833-011-15

Solmara
Lidocaine 4%,Menthol 5%

15
Patches

SOLMARA 
menthol, unspecified form and lidocaine patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69833-011
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol, Unspecified Form (Menthol, Unspecified Form) Menthol, Unspecified Form5 g
Lidocaine (Lidocaine) Lidocaine4 g
Inactive Ingredients
Ingredient NameStrength
2-Ethylhexyl Acrylate 
Methacrylic Acid 
Bentonite 
Sodium Stearate 
Packaging
#Item CodePackage Description
1NDC:69833-011-155 POUCH in 1 CARTON
13 PATCH in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34807/20/2015
Labeler - Spring Hill Therapeutics LLC (079813250)

 
Spring Hill Therapeutics LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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