Tidl Full Body Pain Relief Cryotherapy Spray.

Manufacturer
The Anthos Group, Inc
Effective date
2023-12-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:03:15

Label at a glance#

ProductTidl Full Body Pain Relief Cryotherapy Spray.
Active ingredientMENTHOL
Label structure13 sections

Dosage and administration

·Adults and children 12 years of age and older:Apply to affected area not more than 3 to 4 times daily ·Children under 12 years of age:Consult physician

Label contents#

Full prescribing information#

Active Ingredient

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 arthritis,simple backache,strains and sprains

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

While smoking or near heat or flame

When Using

OTC - WHEN USING SECTION

·avoid contact with the eyes or 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

Stop Use

OTC - STOP USE SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

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

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If accidentally ingested get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

·Adults and children 12 years of age and older:Apply to affected area not more than 3 to 4 times daily
·Children under 12 years of age:Consult physician

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat, Arnica Montana Flower Extract, Beta-Caryophyllene(Clove), Calendula Officinalis Flower Extract, Camellia Sinensis Leaf Extract, Chamomile Recutita Flower Extract, Dimethyl Sulfone, Echinacea Angustifolia Extract, Ilex Paraguariensis Leaf Extract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Oil of Wintergreen, Vanilla Extract, Water

Questions

OTC - QUESTIONS SECTION

Phone:1(888)778-2986

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489073menthol 10.5 % Topical SprayPSN1
1489073menthol 105 MG/ML Topical SpraySCD1
1489073menthol 10.5 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79740-012-012025-01-30C16284748780-11030e365-2152-111a-e063-dadaa90a10e20baa3842-79e2-9735-e063-6294a90ab4ea
79740-012-012024-01-30C16284748780-11030e365-2152-111a-e063-dadaa90a10e20baa3842-79e2-9735-e063-6294a90ab4ea

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79740-012-01Tidl Full Body Pain Relief Cryotherapy Spray.90 mL in 1 BOTTLELIQUID901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79740-012TIDL FULL BODY PAIN RELIEF CRYOTHERAPY SPRAY. (FULL BODY PAIN RELIEF CRYOTHERAPY SPRAY.) LIQUID [THE ANTHOS GROUP, INC]11 package rows20231205_0baa3842-79e2-9735-e063-6294a90ab4ea.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79740-01279740-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
0baa3842-79e3-9735-e063-6294a90ab4ea0baa3842-79e2-9735-e063-6294a90ab4ea2023-12-04WarningsExact identifier
spl id: 0baa3842-79e3-9735-e063-6294a90ab4ea
spl set id: 0baa3842-79e2-9735-e063-6294a90ab4ea

Reported adverse events (FAERS/openFDA)#

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