FDA Label for Activice
View Indications, Usage & Precautions
Activice Product Label
The following document was submitted to the FDA by the labeler of this product Medline Industries, Lp. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Menthol 8.0%
Purpose
Topical Analgesic
Uses
For the temporary relief of minor aches and pains of muscles and joints associated with:
- simple backache
- arthritis
- strains
- bruises
- sprains
Warnings
For external use only.
Avoid contact with eyes.
Flammable: keep away from fire or flame.
Do not puncture or incinerate. Contents under pressure.
When Using This Product
- use only as directed
- do not bandage tightly or use with heating pad
- do not apply to wounds or damaged skin
Stop Use And Ask A Doctor If
- condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
- redness is present
- excessive irritation of the skin develops
If Pregnant Or Breastfeeding,
ask a health professional before use.
Keep Out Of Reach Of Children.
If swallowed, get medical helop or contact a Poison Control Center right away.
Directions
Adults and children over 12 years:
- spray directly onto affected area without the need to rub, massage or bandage
- repeat if necessary, but do not apply more than 4 times daily.
Children 12 years or younger: ask a doctor.
Other Information
- Store at room temperature.
Inactive Ingredients
citric acid, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, peppermint oil, SD alcohol 39C, water.
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