ACTIVICE- menthol liquid 
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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992 ActivICE roll-on

Active Ingredient

Menthol 8.0%

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.

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
  • excessiveirritation 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 over 12
years:

roll 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

Inactive Ingredients

boswellia serrata extract, carbomer,
dimethylsulfone(MSM), eucalyptus oil,
glucosamine sulfate, glycerin,
peppermint oil, SD alcohol 39C,
triethanolamine, water.

Manufacturing Information

Manufactured for:
Medline Industries, LP
Three Lakes Drive, Northfield, IL 60093 USA
Made in USA
www.medline.com
1-800-MEDLINE (633-5463)
REF: MDSAICEROLL, V4 RH23MFO

REF: MDSAICEROLLR, V3 RJ21MFO

Package Labels

Label V4 RH23MFOLabel V3 RJ21MFO

ACTIVICE 
menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-992
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL80 g  in 1000 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER 940 (UNII: 4Q93RCW27E)  
ALCOHOL (UNII: 3K9958V90M)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
TROLAMINE (UNII: 9O3K93S3TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
WATER (UNII: 059QF0KO0R)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-992-6985 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/04/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/04/2019
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 8/2023
Document Id: 03adad6a-32b1-fb1e-e063-6394a90a7f2c
Set id: 8465b443-abe9-78fb-e053-2a91aa0ac1d8
Version: 5
Effective Time: 20230824
 
Medline Industries, LP