79740-006 TIDL Sport Plant Powered Spray

Manufacturer
ANTHOS GROUP, INC, THE
Effective date
2023-01-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:53:05

Label at a glance#

ProductTIDL Sport Plant Powered
Active ingredientMENTHOL
Label structure12 sections

Dosage and administration

Adultsandchildren10yearsofageandolder:Apply to affected area not more than 3 to 4 times daily.·Children un1der 10 years of age:Consult physician.

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

Temporary relief from minor aches and pains of muscles and joints associated with art hrt is, simple backache, strains and sprains

Warnings

WARNINGS SECTION

For external use only.

Flammable:Do not use while smoking or near heat or flame.

When using this product
·avoid contact with the eyes or mucCo US membranes
·do not apply to wounds or damaged skin
·do not appply to the irritated skin
·do not bandage
·wash hands after use wiit hccool water
·do not use with heating pad or device

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

Keep out of reach of children.lf accidentally ingested get medical help or contact a Poison Control Center immediately.

Do not use

OTC - DO NOT USE SECTION

Do not use while smoking or near heat or flame.

OTC - STOP USE SECTION

·condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days.

OTC - WHEN USING SECTION

When using this product
·avoid contact with the eyes or mucCo US membranes
·do not apply to wounds or damaged skin
·do not appply to the irritated skin
·do not bandage
·wash hands after use wiit hccool water
·do not use with heating pad or device

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

Keep out of reach of children.lf accidentally ingested get medical help or contact a Poison Control Center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.lf accidentally ingested get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adultsandchildren10yearsofageandolder:Apply to affected area not more than 3 to 4 times daily.·Children un1der 10 years of age:Consult physician.

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat, Arnica Montana Flower Extract, Calendula Officinalis FlowerExtract, Camellia Sinensis Leaf Extract, Chamomile Recutita Flower Extract, Dimethyl Sulfone, Echinacea Angustifolia Extrac, IIex Paragua riennsis LeafExtract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Oil of Wintergreen, Beta Caryophyllene(Clove), Vanilla Extract, Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79740-006-01 30ml 79740-006-01 30ml79740-006-01 30ml79740-006-02 90ml

79740-006-02 90ml79740-006-02 90ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489073menthol 10.5 % Topical SprayPSN2
1489073menthol 105 MG/ML Topical SpraySCD2
1489073menthol 10.5 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79740-006-01TIDL Sport Plant Powered30 mL in 1 BOTTLESPRAY302
79740-006-02TIDL Sport Plant Powered90 mL in 1 BOTTLESPRAY902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79740-006TIDL SPORT PLANT POWERED (TIDL SPORT PLANT POWERED SPRAY) SPRAY [ANTHOS GROUP, INC, THE]2Legacy NDC, 2 package rows20230111_c28452ce-0ceb-eee0-e053-2995a90a4de2.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79740-00679740-006-01, 79740-006-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
f1e1e29b-c1eb-3eb3-e053-2a95a90af2dac28452ce-0ceb-eee0-e053-2995a90a4de22023-01-09WarningsExact identifier
spl id: f1e1e29b-c1eb-3eb3-e053-2a95a90af2da
spl set id: c28452ce-0ceb-eee0-e053-2995a90a4de2

Reported adverse events (FAERS/openFDA)#

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