Nufabrx Medicine Infused Socks

Manufacturer
Nufabrx LLC
Effective date
2025-10-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:39:01

Label at a glance#

ProductNufabrx Medicine Infused Socks
Active ingredientCAPSAICIN
Label structure8 sections

Indications and uses

Temporary relieves minor pain associated with: arthritis foot, ankle, and calf pain muscle strains sprains bruises cramps

Dosage and administration

clean and dry affected area remove socks from packaging, pull up over calf until snug maximum use of 10 hours per day

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Capsaicin (Nonivamide) 0.11%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporary relieves minor pain associated with:

  • arthritis
  • foot, ankle, and calf pain
  • muscle strains
  • sprains
  • bruises
  • cramps

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • do not wear if you are allergic to any material in this product or chili peppers
  • do not apply to wounds, damaged or irritated skin
  • do not get into eyes or on mucous membranes
  • do not use with heating pad or other external analgesic products
  • a slight burning sensation may occur upon application but generally disappears in several days
  • if severe burning sensation occurs, discontinue use immediately
  • do not use 1 hour prior to bathing or within 30 minutes after bathing

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • conditions worsen
  • severe skin irritation occurs
  • pain persists for more than 7 days
  • symptoms clear up and occur again within a few days

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

Keep out of reach 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 socks from packaging, pull up over calf until snug
  • maximum use of 10 hours per day

Product care instructions

CLEANING, DISINFECTING, AND STERILIZATION INSTRUCTIONS

  • wash separately from other clothes
  • do not store in direct sublight
  • protect product from excessive moisture when not in use

Inactive ingredient

INACTIVE INGREDIENT SECTION

acrylate copolymer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Entire LabelEntire Label

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72490-036-10Nufabrx Medicine Infused Socks1 g in 1 POUCHCLOTH15

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
72490-03672490-036-10

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-11-27full-release2026-06-01 00:39:38

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
Nufabrx Medicine Infused SocksCAPSAICINNufabrx LLC00d7d5bf-ee03-e73d-e063-6394a90a5d942025-10-15WarningsExact identifier
ndc (package): 72490-036-10
ndc (product): 72490-036
ndc11 (package): 72490003610
spl id: 41354184-2390-242b-e063-6394a90a9c8e
spl set id: 00d7d5bf-ee03-e73d-e063-6394a90a5d94

Reported adverse events (FAERS/openFDA)#

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