Toast Screamin Menthol

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 Screamin Menthol
Active ingredientMENTHOL
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

■ Adults and children 12 years of age and older: Rub a thin film over affected areas not more than 4 times daily; massage not necessary. ■ Children under 12 years of age: Consult physician.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

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

Flammable: Keep away from excessive heat or open flame

Ask a doctor before use if you have: Sensitive skin

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes or

mucus membranes ■ do not apply to wounds or damage skin

■ do not use with other ointments creams sprays or ligaments

■ do not apply to irritated skin or if excessive irritation develops

■ do not bandage ■ wash hands after use with cold water

■ do not use with a heating pad or device

Stop using consult a doctor if

OTC - STOP USE SECTION

Condition worsens, or if

symptoms persist for more than 7 days, or clear up in recur

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help

or contact a Poison Control Center immediately.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Adults and children 12 years of age and older: Rub a thin

film over affected areas not more than 4 times daily; massage

not necessary.

■ Children under 12 years of age: Consult physician.

Other information

OTHER SAFETY INFORMATION

■ store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Boswellia Serrata (Frankincense) Extract, Capsicum, Chamomilla Recutita (Matricaria) Flower Extract, Ethylhexylglycerin, Glycerin, Isopropyl Alcohol, Phenoxyethanol, Polysorbate 80, Rosmarinus Officinalis (Rosemary) Leaf Extract, Triethanolamine, 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
1148430menthol 4 % Topical CreamPSN1
1148430menthol 40 MG/ML Topical CreamSCD1
1148430menthol 4 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78983-103-05Toast Screamin Menthol148 g in 1 TUBECREAM1481

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78983-10378983-103-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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 Screamin MentholMENTHOLIDEAZ, LLC37b48b1a-ef3d-afdc-e063-6294a90a66102025-06-16WarningsExact identifier
ndc (package): 78983-103-05
ndc (product): 78983-103
ndc11 (package): 78983010305
spl id: 37b48b35-c838-7f0e-e063-6294a90a0276
spl set id: 37b48b1a-ef3d-afdc-e063-6294a90a6610

Reported adverse events (FAERS/openFDA)#

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