Kwik-moving
FDA Label NDC 73640-019

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by N. N. Impex for the product Kwik-moving (NDC 73640-019). 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, purpose, warning, uses, direction, keep out of reach of children, inactive ingredient, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Eucalyptus Oil 2% , Menthol 5% ,Methyl salicylate 15%

Purpose

External Analgesic

Warning

For external use only.

Allergy alert:If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.


Stop use and ask a doctor if condition
 worsens or if symptoms persist for more than 7 days or clear up and occurs again within a few days. Redness is present. Excessive irritation of the skin develops.

When using this product

Use only as directed. Avoid contact with the eyes or mucous membranes. Do not apply on wounds and damaged skin. Do not bandage tightly. Do not use with heating pad.

If pregnant or breast-feeding, ask a health professional before use.

Uses

For temporary relief of minor aches and pains of muscles and joints due to: simple backaches, bruises, sprains, arthritis

Direction

Adults and children 12 years and older: apply to the affected area and massage gently not more than 3 to 4 times daily.
Children under 12 years of age :consult a physician.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredient

Light liquid paraffin, microcrystalline wax, paraffin wax, turpentine oil

Other Information

Store at room temperature.

Product Label

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