ZIMS MAX FREEZE  PRO FORMULA- menthol, unspecified form liquid 
KOBAYASHI Healthcare International, Inc.

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ZIM'S™ MAX FREEZE
PRO FORMULA

Drug Facts

Active ingredient

Menthol 16%

Purpose

Topical analgesic

Uses

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

Warnings

For external use only

Flammable

Keep away from fire or flame and heated surfaces

Do not use

  • if you are allergic to any ingredient in this product
  • on open wounds, damaged or irritated skin
  • with a heating pad or TENS device
  • after expiration date

When using this product

  • to avoid excess application, press applicator gently against skin
  • do not bandage tightly
  • do not use otherwise than as directed
  • avoid contact with eyes or mucous membranes

Stop use and ask a doctor if

  • condition worsens
  • rash, itching, redness or excessive irritation of the skin develops
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

If pregnant or breast-feeding, 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 12 years of age and over:

Children under 12 years of age:

Other information

Inactive ingredients

†Aloe Barbadensis Leaf Extract, Arnica Extract, Propylene Glycol, SD Alcohol 40-B, Tea Tree Oil, Vanillyl Butyl Ether, Water.

†Symbol before the ingredient indicates certified organic.

Consumer Comments Call: 1-800-432-8629

Distributed by:
KOBAYASHI Consumer Products, LLC
P.O. Box 1191, Dalton, GA 30722

PRINCIPAL DISPLAY PANEL - 89 mL Bottle Carton

ZIM'S™
MAX-
FREEZE
PRO FORMULA

DEEP PENETRATING
PAIN RELIEF

- FAST ACTING
- LONG LASTING
- VANISHING SCENT

Bottle Shaped for
Easy Application

COLD THERAPY
COOLING LIQUID
with 16% Menthol

3 fl oz (89mL)

PRINCIPAL DISPLAY PANEL - 89 mL Bottle Carton
ZIMS MAX FREEZE   PRO FORMULA
menthol, unspecified form liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54273-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM160 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ARNICA MONTANA WHOLE (UNII: O80TY208ZW)  
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)  
TEA TREE OIL (UNII: VIF565UC2G)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54273-009-011 in 1 CARTON08/20/2018
189 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM01708/20/2018
Labeler - KOBAYASHI Healthcare International, Inc. (156391729)

Revised: 11/2023
Document Id: 171be518-73bb-4425-9565-1545166d3f51
Set id: 4d91baf3-9655-4786-93b8-aa0d93fe0bf9
Version: 9
Effective Time: 20231116
 
KOBAYASHI Healthcare International, Inc.