Silvera Pain Relief Patch

Manufacturer
Home Aide Diagnostics, Inc.
Effective date
2014-11-26
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:34:25

Label at a glance#

ProductSilvera Pain Relief Patch
Active ingredientLidocaine, Capsaicin, Menthol
Label structure3 sections

Label contents#

Full prescribing information#

GENERAL PRECAUTIONS SECTION

This product may cause allergic reactions in some individuals.

DRUG FACTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

drugfacts.jpgdrugfacts.jpg

DESCRIPTION SECTION

silverabox.jpgsilverabox.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69379-037-17EA - Each69379-037d1535bf1-ff01-4c32-a2e4-5b34e052c96512015-01-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CapsaicinACTIVE INGREDIENTS07O44R1ZM1
LidocaineACTIVE INGREDIENT98PI2009871
MentholACTIVE INGREDIENTL7T10EIP3A1
CapsaicinACTIVE MOIETYS07O44R1ZM1
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
69379-03769379-037-16, 69379-037-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lidocaine98PI200987ACTIB
CapsaicinS07O44R1ZMACTIB
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
08c94237-533f-40ae-e054-00144ff88e8808c94237-533e-40ae-e054-00144ff88e882014-11-26Exact identifier
spl id: 08c94237-533f-40ae-e054-00144ff88e88
spl set id: 08c94237-533e-40ae-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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