ZIMS MAX FREEZE

Manufacturer
NATURAL ESSENTIALS, INC.
Effective date
2016-02-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:28:12

Label at a glance#

ProductZIMS MAX FREEZE
Active ingredientMENTHOL, LIDOCAINE, MENTHYL SALICYLATE, (+/-)-
Label structure10 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/children 12 years and older Strip off the polyethylene film and place adhesive pad over affected area. Change pad 1 or 2 times a day. Wash Hands after applying patch.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

NATURAL Menthol USP 5%

Lidocaine 4%

Methyl Salicylate 0.04%

PURPOSE:

OTC - PURPOSE SECTION

Topical Analgesic

Topical Analgesic

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

Use only as directed.

  • For external use only

OTC - DO NOT USE SECTION

  • Do Not use if you are allergic to any ingredient in Zim's Max-Freeze Patch
  • Do Not use if you have had allergic reaction to aspirin or other salicylate products
  • Use caution with blood thinning medications, NSAIDS, steroids or nonsteroidal anti-inflammatory drugs
  • If conditions worsens or symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician
  • Avoid contact with eyes or mucous membranes

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • PREGNANCY - Breast Feeding Warning: If pregnant or breastfeeding, ask a physician before use.
  • Do not use with other topical products.
  • Do not use with heating devices.
  • Do not use on open wounds, damaged or irritated skin
  • Keep away from excessive heat.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep this and all medicine out of reach of children.
  • Accidental ingestion: Seek professional help and contact Poison Control immediately
  • Under age 12 Consult a physician before use.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults/children 12 years and older

  • Strip off the polyethylene film and place adhesive pad over affected area.
  • Change pad 1 or 2 times a day.
  • Wash Hands after applying patch.

OTHER:

OTHER SAFETY INFORMATION

Store at room temperature - do not exceed 86° Fahrenheit

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

†Aloe Barbadensis Leaf Extract, Aluminum Hydroxide, Alcohol, Arnica Extract, Borneol, Camphor, EDTA-2Na, Glycerin, NP-700, PVPP, Tartaric Acid, Titanium Dioxide, Water.

Distributed by: Perfecta Products, Inc., North Lima, OH 44452

(800) 319-2225-www.ZimsUSA.com

©2015 Perfecta Products, Inc.®

Principal Display Panel - Medium Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZIM's

MAX

FREEZE

PATCHES

MUSCLE & JOINT*

Description: Zim's Max-Freeze Patch

Size: Medium

Lot#: 123456

Expiration Date - 1/1/19

Principal Display Panel - Medium Pouch Label
Principal Display Panel - Medium Pouch Label

Principal Display Panel - Large Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZIM's

MAX

FREEZE

PATCHES

MUSCLE & JOINT*

Description: Zim's Max-Freeze Patch

Size: Large

Lot#: 123456

Expiration Date - 12/25/18

Principal Display Panel - Large Pouch Label
Principal Display Panel - Large Pouch Label

Principal Display Panel - Extra Large Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZIM's

MAX

FREEZE

PATCHES

MUSCLE & JOINT*

Description: Zim's Max-Freeze Patch

Size: Extra Large

Lot#: 123456

Expiration Date - 1/5/19

Principal Display Panel - Extra Large Pouch Label
Principal Display Panel - Extra Large Pouch Label

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66902-11366902-113-06, 66902-113-04, 66902-113-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2b0f0042-f21d-174f-e063-6394a90a40abce4a477a-f947-422e-85ac-72b16f7b92f22025-01-06WarningsExact identifier
spl set id: ce4a477a-f947-422e-85ac-72b16f7b92f2

Reported adverse events (FAERS/openFDA)#

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