Active Ingredient
Menthol 10.0%
Activice Spray
FDA Label NDC 53329-996
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Medline Industries, Lp for the product Activice (NDC 53329-996). 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 ingredient, purpose, uses, warnings, when using this product, stop use and ask doctor if, if pregnant or breastfeeding,, keep our of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 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 Our Of Reach Of Children.
If swallowed, get medical help 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
- ask a doctor
Children 12 years or younger:
Other Information
- store at room temperature
Inactive Ingredients
boswellia serrata extract, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, glycerine, SD alcohol 39C, PEG-8 dimethicone, pentylene glycol, peppermint oil, water (USP)
Manufacturing Information
REF: MDSAICESPRY4
Not made with Natural Rubber Latex.
www.medline.com Manufactured in USA for: Medline Industries, Inc.
Three Lakes Drive, Northfield, IL 60093 1-800MEDLINE
*This product is not manufactured or distributed by Performance Health and/or its subsidiaries, owner of the registered trademark Biofreeze®.
Package Label
Pdp (53329 996 Mdsaicespry42)
* Please review the disclaimer below.
