FDA.reportPublic FDA data

Medicated Compression Sock

Manufacturer
Textile-Based Delivery, Inc.
Effective date
2019-12-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:02:03

Label at a glance#

ProductMedicated Compression Sock
Active ingredientCAPSAICIN
Label structure8 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache,arthritis, strains, bruises and sprains.

Dosage and administration

Clean and dry affected area Remove product and put on body Maximum use of 8 hours per day Do not wear more than 4 days per week without doctor consent Wash separately for best results

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Synthetic Capsaicin 0.13%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache,arthritis, strains, bruises and sprains.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • Allergy Alert: if you are allergic to any ingredients of this product or chili peppers contact a doctor before use
  • On wounds or damaged skin
  • With, or at same time as, other external analgesic products
  • With a heating pad

When using this product

OTC - WHEN USING SECTION

  • You may experience a burning sensation which is normal and related to the way the product works. With regular use, this sensation generally diminishes.
  • Do not use immediately before or after activities such as swimming, showering, or sunbathing.
  • Use only as directed.
  • Avoid contact with eyes and mucous membranes or rashes.
  • Wash hands after putting product on body and before touching your face or eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens, symptoms persist more than 7 days or clear up and occur again within a few days.
  • rash, itching or excessive skin irritation develops.
  • If pregnant or breastfeeding consult a healthcare professional before use.

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

  • Clean and dry affected area
  • Remove product and put on body
  • Maximum use of 8 hours per day
  • Do not wear more than 4 days per week without doctor consent
  • Wash separately for best results

Other Information

SPL UNCLASSIFIED SECTION

Avoid storing product in direct sunlight. Protect product from excessive moisture

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylate copolymer

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

006pdp006pdp

006df006df

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72490-006-012023-01-30C16284748780-1f386c64a-1449-0266-e053-dadaa90a7c1aMedicated Compression Socks
72490-006-022023-01-30C16284748780-1f386c64a-1449-0266-e053-dadaa90a7c1aMedicated Compression Socks
72490-006-032023-01-30C16284748780-1f386c64a-1449-0266-e053-dadaa90a7c1aMedicated Compression Socks

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72490-006-01Medicated Compression Sock2 in 1 POUCHCLOTH22
72490-006-02Medicated Compression Sock2 in 1 POUCHCLOTH22
72490-006-03Medicated Compression Sock2 in 1 POUCHCLOTH22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72490-006MEDICATED COMPRESSION SOCK (CAPSAICIN) CLOTH [TEXTILE-BASED DELIVERY, INC.]2Legacy NDC, 3 package rows20191218_8dd1337b-dd80-afd7-e053-2a95a90a3cc2.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72490-00672490-006-01, 72490-006-02, 72490-006-03

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
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
CAPSAICINS07O44R1ZMACTIB

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
99eae796-3ff1-2a98-e053-2995a90a79fe8dd1337b-dd80-afd7-e053-2a95a90a3cc22019-12-17WarningsExact identifier
spl id: 99eae796-3ff1-2a98-e053-2995a90a79fe
spl set id: 8dd1337b-dd80-afd7-e053-2a95a90a3cc2

Reported adverse events (FAERS/openFDA)#

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