DZUL PAIN FREEZE

Manufacturer
Caball Sales, Inc.
Effective date
2026-03-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:51:49

Label at a glance#

ProductDZUL PAIN FREEZE INSTANT PAIN RELIEF
Active ingredientMENTHOL
Label structure13 sections

Dosage and administration

Adults and Children over 12 years of age Spray two to three pumps or as necessary to cover the affected area not more than three to four times daily. Children under 12 years of age: do not use, consult a doctor.

Storage and handling

Store tightly closed in a dry place at controlled room temperature between 59-86 F (15°-30° C).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.5%

OTC - PURPOSE SECTION

Topical Analgesic

USE

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints.

WARNINGS SECTION

For external use only.

Do not apply to wounds or damaged skin, with a heating pad or on a child under 12 years of age.

Flammable

SAFE HANDLING WARNING SECTION

Keep away from fire or flame.

OTC - WHEN USING SECTION

Use only as directed.
Do not bandage tightly.
Avoid contact with eyes and mucous membranes.
If you experience an allergic reaction, discontinue use, and consult a doctor.

Do not expose the area treated with product to heat or direct sunlight.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Condition worsens.
Redness is present.
Irritation develops.
Symptoms persist for more than 7 days or clear up occur again within a few days.

You experience signs of injury, such as pain, swelling or blistering where the product was applied.

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

If swallowed, get medical help, or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years of age

Spray two to three pumps or as necessary to cover the affected area not more than three to four times daily.

Children under 12 years of age: do not use, consult a doctor.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store tightly closed in a dry place at controlled room temperature between 59-86 F (15°-30° C).

INACTIVE INGREDIENT SECTION

Alcohol Denat, Glycerin, Propylene Glycol, Aloe Barbadensis (Aloe Vera) Leaf Juice.

DZUL PAIN FREEZE INSTANT PAIN RELIEF

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PAIN RELIEFPAIN RELIEF

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850019307597GTIN-13: 0850019307597
EAN-13: 0850019307597
GTIN-12: 850019307597
UPC-A: 850019307597
GTIN storage (14 digits): 00850019307597
DZUL - PAIN FREEZE INSTANT PAIN RELIEF 3-27-2026.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83037-510-04DZUL PAIN FREEZEINSTANT PAIN RELIEF118 mL in 1 BOTTLE, SPRAYSPRAY1182

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83037-51083037-510-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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
DZUL PAIN FREEZE INSTANT PAIN RELIEFMENTHOLCaball Sales, Inc.4df3abcc-17f3-17f2-e063-6294a90afcca2026-03-26WarningsExact identifier
ndc (package): 83037-510-04
ndc (product): 83037-510
ndc11 (package): 83037051004
spl id: 4df3abd7-8212-9725-e063-6394a90a557c
spl set id: 4df3abcc-17f3-17f2-e063-6294a90afcca

Reported adverse events (FAERS/openFDA)#

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