Label: GADADERM FROZEN ICE ADVANCE PAIN RELIEF (salicylic acid menthol camphor- natural gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated November 18, 2016

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENTS
    Active IngredientsPurpose - Methyl Salicylate 10%Topical Analgesic - Menthol 10%Topical Analgesic - Camphor 3.1%Topical Analgesic
  • INACTIVE INGREDIENT
    Carbopol, Cetearyl Alcohol, Disodium EDTA, FD&C Blue #1, Glycerin, Hydroxypropyl Methylcellulose, Menthylparaben, Propylene Glycol, Propylparaben, Polysorbate 20, Purified Water, Stearic Acid ...
  • KEEP OUT OF REACH OF CHILDREN
  • INDICATIONS & USAGE
  • WARNINGS
    For the external use only. When using this product use as directed. Do not bandage tightly or use with heating pad. Avoid contact with eyes and mucous membranes. Do not apply to wounds or ...
  • DOSAGE & ADMINISTRATION
    Adults and children 12 years of age and older; apply generously to affected area massage into painful area until thoroughly absorbed into skin. Repeat as necessary but not more than 3 to 4 times ...
  • PURPOSE
    For temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains.
  • GADADERM Frozen Ice Advance Pain Relief
    Label Image
  • INGREDIENTS AND APPEARANCE
    Product Information
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!