Toast Freezin Cold

Manufacturer
IDEAZ, LLC
Effective date
2025-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:03:13

Label at a glance#

ProductToast Freezin Cold
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure9 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints associated with ■ arthritis ■ strains ■ bruises ■ sprains

Dosage and administration

■ Use only as directed ■ adults and children 12 years of age or older: apply to affected area not more than 3 to 4 times daily ■ children under 12 years of age: consult a physician

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 11%

Methyl Salicylate 31%

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 ■ arthritis ■ strains

■ bruises ■ sprains

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on wounds ■ on damaged skin

■ immediately before or after bathing or using a hot tub

■ with a heating pad ■ under wrapping or bandage

where perspiration is likely to occur

When using this product

OTC - WHEN USING SECTION

■ Avoid contact with eyes

and mucous membranes ■ do not bandage tightly

Stop using consult a doctor if

OTC - STOP USE SECTION

■ Condition worsens or

symptoms persist for more than 7 days ■ symptoms clear up

and occur within a few days ■ excessive skin irritation occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Use only as directed

■ adults and children 12 years of age or older:

apply to affected area not more than 3 to 4 times daily

■ children under 12 years of age: consult a physician

Other information

OTHER SAFETY INFORMATION

■ Store between 20-25° C (68-77°F) ■ protect from freezing

Inactive ingredients

INACTIVE INGREDIENT SECTION

Behentrimonium Methosulfate, Boswellia Serrata Extract, Butylene Glycol, Cetyl Alcohol, Chamomilla Recutita (Matricaria) Flower, Ethylhexylglycerin, Glycerin, Phenoxyethanol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Water

Questions or Comments?

OTC - QUESTIONS SECTION

1-800-4NO-PAIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1300276menthol 11 % / methyl salicylate 31 % Topical CreamPSN1
1300276menthol 110 MG/ML / methyl salicylate 310 MG/ML Topical CreamSCD1
1300276menthol 11 % / methyl salicylate 31 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78983-104-05Toast Freezin Cold148 g in 1 TUBECREAM1481

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78983-10478983-104-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
Toast Freezin ColdMENTHOL, METHYL SALICYLATEIDEAZ, LLC37b4d363-0099-8cd3-e063-6394a90a18d62025-06-16WarningsExact identifier
ndc (package): 78983-104-05
ndc (product): 78983-104
ndc11 (package): 78983010405
spl id: 37b4d302-653c-ddbd-e063-6294a90a7ef6
spl set id: 37b4d363-0099-8cd3-e063-6394a90a18d6

Reported adverse events (FAERS/openFDA)#

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