Otc - Active Ingredient
Camphor 4% .……..…….............….. Topical Analgesic
Menthol 10% ...……......……….....… Topical Analgesic
Methyl Salicylate 30% .......….......… Topical Analgesic
Pain Relieving
FDA Label NDC 24488-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Creation's Garden Natural Products, Inc for the product Pain Relieving (NDC 24488-001). 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 otc - active ingredient, uses, warnings, directions, inactive ingredients, questions?, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
■ Temporarily relieves the minor aches and pains of
muscles and joints associated with: ■ arthritis
■ strains ■ bruises ■ sprains ■ backache
Warnings
For external use only
Do not use: ■ on wounds or damaged skin
■ with a heating pad ■ on a child under 12 years of
age with arthritis like conditions
Directions
Directions
■ Use only as directed
■ Adults and children 12 years of age and older apply
to affected area not more than 3 to 4 times daily
■ Children under 12 years of age ask a doctor
Inactive Ingredients
Inactive ingredients
water, carbomer, disodium edta, glyceryl stearate se,
lanolin, polysorbate 80, stearic acid, triethanolamine,
potassium hydroxide
Questions?
Questions? Call 1-866-923-4914
Package Label.Principal Display Panel
Image Of Tube Label (Dr 2oz Us Painrelievingcrm Lbl R2)
Image Of Carton Label (Dr 2oz Us Painrelievingcrm Crt R2)
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