Active Ingredients:
Menthol 10.00%
Camphor 3.00%
Arctic Blast Pain Releiving Liquid
FDA Label NDC 71856-176
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nutriomo Labs Pte, Ltd for the product Arctic Blast Pain Releiving (NDC 71856-176). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients:, indications:, warnings:, keep out of reach of children., do not apply, if pregnant or breast feeding,, directions:, additional information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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, discontine 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:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Emu Oil, Dimethyl Sulfoxide (DMSO), Ethylhexylglycerin, Hypericum Perforatum (St. John's Wort) Oil, Olea Europaea (Olive) Oil, Phenoxyethanol, Polysorbate-20, SD-Alcohol 40B.
Package Labeling:
Label (Label)
* Please review the disclaimer below.
