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Dusel Warm Arthritis Dead Sea Salt Therapy

Medically reviewed on February 16, 2017

Dosage form: cream
Ingredients: CAPSAICIN 0.25mg in 1mL
Labeler: Nanovita One LLC
NDC Code: 70656-741

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.

Dusel Warm Arthritis Dead Sea Salt Therapy

Drug Facts:

Active Ingredient:

Capsaicin 0.025%

Topical Analgesic

Indications:

For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.

Warnings:

• For external use only.
• Avoid contact with eyes.
• If symptoms persist for more than seven days, discontinue use and consult physician

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 prior to use.

Directions:

•Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.
•Children under two-years of age: consult a physician.

Additional Information:

Store at room temperature.

Other Ingredients:

Aqua (Deionized Water), Ethylhexylglycerin, Helianthus Annuus (Sunflower) Oil, Hydroxyethylcellulose Isopropyl Myristate, Maris Sal (Dead Sea) Salt, Phenoxyethanol, Polysorbate-20, Sea (Dead) Salt, (Corn) Zemea Propanediol.

Package Labeling:

DUSEL WARM ARTHRITIS DEAD SEA SALT THERAPY 
capsaicin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70656-741
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAPSAICIN (CAPSAICIN) CAPSAICIN0.25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ETHYLHEXYLGLYCERIN 
HELIANTHUS ANNUUS FLOWERING TOP 
PHENOXYETHANOL 
POLYSORBATE 20 
SEA SALT 
CORN 
Packaging
#Item CodePackage Description
1NDC:70656-741-015 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/26/2016
Labeler - Nanovita One LLC (080217774)

 
Nanovita One LLC

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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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