FDA.reportPublic FDA data

Veltrix Pain Relieiving Cream

Manufacturer
Home Aide Diagnostics, Inc. | Zhejiang Bangli Medical Products Cl. Ltd.
Effective date
2015-07-13
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:20:58

Label at a glance#

ProductVeltrix
Active ingredientLIDOCAINE, MENTHOL
Label structure7 sections

Label contents#

Full prescribing information#

INFORMATION FOR PATIENTS SECTION

PURPOSE: Topical analgesic


ACTIVE INGREDIENTS
Lidocain 4% --------------------------------------------------------------------------------------------------------- Topical analgesic
Menthol 1% --------------------------------------------------------------------------------------------------------- Topical analgesic

INDICATIONS & USAGE SECTION

INDICATIONS
For the temporary relief of pain of muscles and joints associated with:

  • Arthritis
  • Simple Backache
  • Strains
  • Sprains
  • Bruises

DIRECTIONS
Adults and children over 12 years
Apply generously to affected area
Massage into painful area until thoroughly absorbed into skin, repeat as necessary, not more than 3-4 times daily
Store at 20°-25°C (68°-77 °F). Avoid direct sunlight.

WARNINGS SECTION

WARNINGS
FOR EXTERNAL USE ONLY.

  • When using this product use only as directed
  • Do not bandage tightly
  • Do not use with a heating pad
  • Agoid contact with the eyes or mucous membranes
  • Do not apply to wounds or damaged or irritated skin

WARNINGS AND PRECAUTIONS SECTION

STOP USE AND ASK A DOCTOR IF

  • Condition worsens
  • Symptoms persist for more than 7 days or clear up and occur again within a few days
  • Redness is present
  • Irritation develops

OTHER SAFETY INFORMATION

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
  • If pregnant of breast-feeding, ask a healthcare professional before use

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS
aliphatic alcohol; stearic acid; vaseline; peregal; Carmellose; odium; water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VeltrixRX.jpgVeltrixRX.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
250912lidocaine 4 % / menthol 1 % Topical CreamPSN1
250912lidocaine 40 MG/ML / menthol 10 MG/ML Topical CreamSCD1
250912lidocaine 4 % / menthol 1 % Topical CreamSY1

DailyMed Pharmacologic Classes#

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130169379004030GTIN-13: 0169379004030
EAN-13: 0169379004030
GTIN-12: 169379004030
UPC-A: 169379004030
GTIN storage (14 digits): 00169379004030		VeltrixRX.jpg

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
69379-004-032020-01-31C16284748780-19d75b9d0-9f16-f424-e053-dadaa90a57ceVeltrix Pain Relieiving Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69379-004-03Veltrix120 g in 1 BOTTLECREAM1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69379-004VELTRIX (VELTRIX PAIN RELIEIVING CREAM) CREAM [HOME AIDE DIAGNOSTICS, INC.]1Legacy NDC, 1 package rows20150713_1ac45dcf-6100-1a8b-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
LIDOCAINEACTIVE INGREDIENT98PI2009871
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
LIDOCAINEACTIVE MOIETY98PI2009871
MENTHOLACTIVE MOIETYL7T10EIP3A1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69379-00469379-004-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIDOCAINE98PI200987ACTIB
MENTHOLL7T10EIP3AACTIB

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
1ac45dcf-6101-1a8b-e054-00144ff8d46c1ac45dcf-6100-1a8b-e054-00144ff8d46c2015-07-13WarningsExact identifier
spl id: 1ac45dcf-6101-1a8b-e054-00144ff8d46c
spl set id: 1ac45dcf-6100-1a8b-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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