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 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

Children 12 years or younger:

ask a doctor

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

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:53329-996
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:53329-996-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	01/01/2020

Labeler - Medline Industries, LP (025460908)

Registrant - Medline Industries, LP (025460908)

996 ActivICE™ Extra Strength Temporary Pain Relief, Spray