ACTIVICE- menthol spray 
Medline Industries, LP

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.

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996 ActivICE™ Extra Strength Temporary Pain Relief, Spray

Active ingredient

Menthol 10.0%

Purpose

Topical analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with:

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:

Children 12 years or younger:

Other information

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

Manufactured for:
Medline Industries, LP
Three Lakes Drive, Northfield, IL 60093 USA
Made in USA with
www.medline.com
1-800-MEDLINE (633-5463)
REF: MDSAICESPRY4
V3 RF23MFO

*This product is not manufactured or distributed by Performance Health and/or its subsidiaries, owner of the registered trademark Biofreeze®.

Package Label

Label V3 RF23MFO

ACTIVICE 
menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-996
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
ALCOHOL (UNII: 3K9958V90M)  
PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
GLYCERIN (UNII: PDC6A3C0OX)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
WATER (UNII: 059QF0KO0R)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-996-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/2020
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 8/2023
Document Id: 037657d1-8d93-d960-e063-6394a90ae5ea
Set id: 98fa9a34-0e1e-0997-e053-2a95a90ac77d
Version: 4
Effective Time: 20230821
 
Medline Industries, LP