FDA.reportPublic FDA data

Lidoxi

Manufacturer
T&T Pharma Holdings LLC
Effective date
2026-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:31

Label at a glance#

ProductLidoxi
Active ingredientLIDOCAINE
Label structure10 sections

Indications and uses

For the temporary relief of muscle pain and joint pain associated with: -Backache -Cramps -Soreness -Strains -Discomfort -Neckache

Dosage and administration

Adults and Children 12 Years of Age and Older - Clean and dry the affected area before treatment - Apply up to 4 times daily - Wash hands immediately after use

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Local Anesthetic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of muscle pain and joint pain associated with:
-Backache -Cramps -Soreness -Strains -Discomfort -Neckache

Warnings:

WARNINGS SECTION

For External Use Only

Allergy Alert

SPL UNCLASSIFIED SECTION

Local anesthetics may cause methemoglobinemia. If an allergic reaction occurs, stop use and seek medical attention immediately.

Do Not Use

OTC - DO NOT USE SECTION

- On damaged, irritated, or infected skin
- With a bandage or heating pad
- If you are allergic to any ingredients in this product
- In the eyes, nose, or mouth
- Otherwise as directed

When Using This Product

OTC - WHEN USING SECTION

Avoid contact with the eyes, nose, and mouth

Stop Use and Ask Doctor If

OTC - STOP USE SECTION

- Any of the Warnings apply to you
- Excessive skin irritation develops
- Condition worsens
- Symptoms persist for more than 7 days, or symptoms clear up and occur aqain within 3 days

If Pregnant or Breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a healthcare professional before use

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested seek medical help or contact a Poison Control Center immediately

Flammable

SPL UNCLASSIFIED SECTION

Keep away from excessive heat or open flame

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and Children 12 Years of Age and Older
- Clean and dry the affected area before treatment
- Apply up to 4 times daily
- Wash hands immediately after use

Other Information

SPL UNCLASSIFIED SECTION

- Store in a cool, dry place with lid tightly closed. Keep from freezing.
- If the tamper-evident foil seal is not intact, do not use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate, Ascorbic
Acid, Amica Montana Flower Extract, Boswellia Serrata Gum Extract, Capric
Triglyceride, Cetyl Alcohol, Cinnamomum Zeylanicum (Cinnamon) Extract,
Curcuma Longa Root Extract, Dimethicone, Dimethyl Sulfoxide, Ethylhexylglycerin,
Eucalyptus Globulus Leaf Oil, Glycerin, Glyceryl Stearate, lnulin Lauryl Carbamate,
PEG-100 Stearate, Phenoxyethanol, Stearic Acid, Tetrasodium EDTA, Tocopherol,
Triethanolamine, Water.

Questions or Comments:

OTC - QUESTIONS SECTION

info@ttpharmarx.com

Package - 92g Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tubetube

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2559400lidocaine 4 % Topical OintmentPSN1
2559400lidocaine 0.04 MG/MG Topical OintmentSCD1
2559400lidocaine 4 % Topical OintmentSY1

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
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87239-1111-1Lidoxi92 g in 1 TUBE, WITH APPLICATOROINTMENT921

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87239-111187239-1111-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
GLYCERYL STEARATE230OU9XXE4IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATEKBC00G95HIIACT
BOSWELLIA SERRATA GUM4PW41QCO2MIACT
EUCALYPTUS GLOBULUS LEAF OIL2R04ONI662IACT
STEARIC ACID4ELV7Z65APIACT
INULIN LAURYL CARBAMATE48RFF58ESGIACT
TRIETHANOLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
TOCOPHEROLR0ZB2556P8IACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CETYL ALCOHOL936JST6JCNIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TETRASODIUM EDTAMP1J8420LUIACT
TRICAPRINO1PB8EU98MIACT
PEG-100 STEARATEYD01N1999RIACT
LIDOCAINE98PI200987ACTIB
ETHYLHEXYLGLYCERIN147D247K3PIACT
CURCUMA LONGA (TURMERIC) ROOT856YO1Z64FIACT
CINNAMOMUM ZEYLANICUM BARK OILXE54U569ECIACT
DIMETHICONE92RU3N3Y1OIACT
DIMETHYL SULFOXIDEYOW8V9698HIACT

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
LidoxiLIDOCAINET&T Pharma Holdings LLC513c517e-c098-02aa-e063-6294a90ac8a42026-05-07WarningsExact identifier
ndc (package): 87239-1111-1
ndc (product): 87239-1111
ndc11 (package): 87239111101
spl id: 513c517e-c099-02aa-e063-6294a90ac8a4
spl set id: 513c517e-c098-02aa-e063-6294a90ac8a4

Reported adverse events (FAERS/openFDA)#

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