ZIMS MAX FREEZE

Manufacturer: KOBAYASHI Healthcare International, Inc. | KOBAYASHI America Manufacturing, LLC
Effective date: 2022-12-07
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: legacy-cache
Hydrated at: 2026-08-01 21:45:06

Label at a glance#

ProductZIMS MAX FREEZE

Active ingredientMENTHOL, UNSPECIFIED FORM

Label structure11 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: Simple backache Arthritis Strains Bruises Sprains

Dosage and administration

Adults and children 12 years of age and over: spray affected area not more than 4 times daily no need to rub wash hands after each use with cold water Children under 12 years of age: consult a doctor

Storage and handling

store in a cool place away from direct sunlight store with cap closed tightly

Contacts and useful links#

PhoneLabel contact800-319-2225

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Natural Menthol USP 3.7%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

Simple backache
Arthritis
Strains
Bruises
Sprains

Warnings

WARNINGS SECTION

For external use only

Flammable

SPL UNCLASSIFIED SECTION

Keep away from fire or flame and heated surfaces

OTC - DO NOT USE SECTION

Do not use

if you are allergic to any ingredient in Zim's Max-Freeze
on open wounds, damaged or irritated skin
with a heating pad or TENS device
near face
after expiration date

OTC - WHEN USING SECTION

When using this product

do not bandage tightly
do not use otherwise than as directed
avoid contact with eyes or mucous membranes

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

SPL UNCLASSIFIED SECTION

CONTENTS UNDER PRESSURE. DO NOT PUNCTURE OR INCINERATE.
DO NOT STORE ABOVE 120°F (48°C)

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over:

spray affected area not more than 4 times daily
no need to rub
wash hands after each use with cold water

Children under 12 years of age: consult a doctor

Other information

STORAGE AND HANDLING SECTION

store in a cool place away from direct sunlight
store with cap closed tightly

Inactive ingredients

INACTIVE INGREDIENT SECTION

†Aloe Barbadensis Leaf Extract, †Arnica Extract, Camphor, †Ilex Paraguariensis Leaf Extract, SDA-39C, Tea Tree Oil, Tocopheryl Acetate (Vitamin E Acetate), Water.

†Symbol before the ingredient indicates certified organic.

OTC - QUESTIONS SECTION

Consumer Comments Call: 800-319-2225

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 109 g Can Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZIM'S™
MAX-
FREEZE

ADVANCED FORMULA
- Muscle & Joint -
PAIN RELIEF

Greaseless, vanishing
scent with organic
ilex, aloe & arnica plus
vitamin e and tea tree oil.

Paraben & sulfate free.

Continuous
Multi-Way Spray

CONTINUOUS
COOLING SPRAY
with Menthol

Net Wt 3.9 oz (109g)

PRINCIPAL DISPLAY PANEL - 109 g Can Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

ZIMS MAX FREEZE
MENTHOL, UNSPECIFIED FORM
ALCOHOL
ALOE VERA LEAF
ARNICA MONTANA WHOLE
CAMPHOR (SYNTHETIC)
ILEX PARAGUARIENSIS LEAF
TEA TREE OIL
.ALPHA.-TOCOPHEROL ACETATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54273-004	54273-004-01, 54273-004-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL, UNSPECIFIED FORM	L7T10EIP3A	ACTIB
ALCOHOL	3K9958V90M	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ARNICA MONTANA WHOLE	O80TY208ZW	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	IACT
ILEX PARAGUARIENSIS LEAF	1Q953B4O4F	IACT
TEA TREE OIL	VIF565UC2G	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
7aaec8a1-fa38-41f6-8e72-63e88b1d1563			a30fd8fa-30a5-4cc3-a25f-acded206152e	2022-12-07	Warnings	Exact identifier spl id: 7aaec8a1-fa38-41f6-8e72-63e88b1d1563 spl set id: a30fd8fa-30a5-4cc3-a25f-acded206152e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.