ActivICE
- Dosage form
- SPRAY
- Labeler
- Medline Industries, LP
- Label updated
- 2025-10-23
- Retrieved
- 2026-09-07
- Active ingredients
- MENTHOL
Active ingredient
Menthol 10.0%
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 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 help or contact a Poison Control Center right away.
Directions
Adults and children 2 years of age and older:
- spray directly onto affected area without the need to rub, massage or bandage
- repeat if necessary, but do not apply more than 3 to 4 times daily
- wash hands after use.
Children under 2 years of age:
- do not use, consult a doctor.
Other information
- store at room temperature
Inactive ingredients
boswellia serrata extract, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, glycerine, PEG-8 dimethicone, pentylene glycol, peppermint oil, SD alcohol 39C, water (USP)
Questions or comments?
1-800-MEDLINE (633-5463)
Manufacturing information
REF: MDSAICESPRY4
Not made with Natural Rubber Latex. Keep product upright. Handle with care. Protect from freezing, avoid excessive heat.
www.medline.com Manufactured in USA for: Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA. 1-800-MEDLINE
*This product is not manufactured or distributed by Reckitt Benckiser Group PLC and/or its subsidiaries, owner of the registered trademark Biofreeze®.
Label information
Changes to the indications and usage section on April 2026
Package Label
[Image in the official label — see DailyMed source]
DailyMed Set ID: 98fa9a34-0e1e-0997-e053-2a95a90ac77d · Version 6
NDC: 53329-996