SUNMED MOTION

Manufacturer
Sunflora Inc
Effective date
2019-08-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:09

Label at a glance#

ProductSUNMED MOTION
Active ingredientLIDOCAINE
Label structure8 sections

Indications and uses

Temporarily relieves minor pain associated with: • arthritis  • sprains  • simple backache  • muscle strains  • cramps  • bruises

Dosage and administration

• Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily. • Children under 2 years of age: Consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain associated with:

• arthritis  • sprains  • simple backache  • muscle strains  • cramps  • bruises

Warnings

WARNINGS SECTION

For external use only

When using this product

• use only as directed • do not bandage tightly • avoid contact with eyes • do not apply to wounds or damaged skin • do not use in large  quantities, particularly over raw surfaces or blistered areas.

Stop use and ask a doctor if

• condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily.

• Children under 2 years of age: Consult a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Allantoin, Caprylic/Capric Triglyceride, Capsicum Annuum Fruit Powder, Calcium Disodium EDTA, Cannabis Sativa (Aerial) Extract Oil, Dimethicone, dl-alpha Tocopheryl Acetate, Ethyl Alcohol, Ethylhexylglycerin, Ethylhexyl Stearate, Fragrance, Glycerin, Phenoxyethanol, Polysorbate 80, Propanediol, Propylene Glycol, Purified Water, Simethicone, Sodium Polyacrylate, Trideceth-6, Vitis Vinifera (Grape) Seed Oil, Xanthan Gum.

SPL UNCLASSIFIED SECTION

Visit us at SUNFLORA.org

This product has not been evaluated by the Food & Drug Administration and is not intended to diagnose, treat, cure, or prevent any disease. Consult your physician before use. For adults 18+.

DISTRIBUTED BY:

SunFlora, Inc.
411 19th street S

St.  Petersberg, FL 

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2197844lidocaine 4 % Topical SolutionPSN1
2197844lidocaine 40 MG/ML Topical SolutionSCD1
2197844lidocaine 4 % Topical SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73240-902-112022-01-28C16284748780-1d6a99b39-ec28-a426-e053-dadaa90af4c2SUNMED MOTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73240-902-11SUNMED MOTION1 in 1 BOXLIQUID11
73240-902-11SUNMED MOTION74 mL in 1 BOTTLELIQUID741

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73240-902SUNMED MOTION (LIDOCAINE) LIQUID [SUNFLORA INC]1Legacy NDC, 2 package rows20190828_1ef36715-2b45-441e-9f61-d99b8d553d11.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73240-90273240-902-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
ab6d01ad-61f7-438b-ae5b-57ab51156bb61ef36715-2b45-441e-9f61-d99b8d553d112019-08-22WarningsExact identifier
spl id: ab6d01ad-61f7-438b-ae5b-57ab51156bb6
spl set id: 1ef36715-2b45-441e-9f61-d99b8d553d11

Reported adverse events (FAERS/openFDA)#

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