SUNMED pain spray Fast-Acting with MENTHOL

Manufacturer
Sunflora Inc. | Inspec Solutions LLC.
Effective date
2025-08-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:11:11

Label at a glance#

ProductSUNMED pain freeze
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol ................ 6%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Temporary relief from minor aches and pains of muscles and joints associated with arthritis,simple backache,strains and sprains.

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product • avoid contacts with the eyes Of mucous membranes • do not apply to wounds or damaged skin • do not apply to irritated skin • do not bandage • wash hands after use with cool water • do not use with heating pad or device.

OTC - STOP USE SECTION

Stop use and ask doctor if condition worsens or symptoms persist for more than 7 days, or clear up and reoccur a gain within few days.

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 immediately

DOSAGE & ADMINISTRATION SECTION

Directions: Adult and children 2 years of age and older. Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age consult a physician

INACTIVE INGREDIENT SECTION

Inactive ingredients /Joo Barbadensis Leaf Extract,Arcium Lappa Roof (Buroock) Extract, Amica Montana Flower Extract, Boswellia Carteni Resin Extract Calendu Officinalis Extract, Camellia Sinensis Leaf Extract,Camphor; CartJomer,FD&C Blue #1,FD&C Yellow #5,Glycenn,llex Paraguanensis (Mate) Leaf Extract oopropyf /Jcoh , oopropyf Myristafe,Melissa Officinalis (LemooBalm)Leaf Extract, Silica,T=heryf Acetate,Tnethanolamine,water,Whole Hemp Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sunmed Pain-Freeze Gel with MentholSunmed Pain-Freeze Gel with Menthol

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73240-904-012025-08-19C16284748780-12cef2736-7e50-d83d-e063-dadaa90ab31fSUNMED pain spray Fast-Acting with MENTHOL
73240-904-012025-01-30C16284748780-12cef2736-7e50-d83d-e063-dadaa90ab31fSUNMED pain spray Fast-Acting with MENTHOL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73240-904-01SUNMED pain freeze89 mL in 1 BOTTLE, PLASTICSPRAY892

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73240-90473240-904-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
55939cdd-a20d-c919-e063-6294a90a6832ff49699c-ced9-13d2-e053-6394a90af0792026-07-01WarningsExact identifier
spl set id: ff49699c-ced9-13d2-e053-6394a90af079

Reported adverse events (FAERS/openFDA)#

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