FDA.reportPublic FDA data

NeuroComfort Pain Relief Roll-on Extra Strength

Manufacturer
ABACUS HEALTH PRODUCTS, INC. | Inspec Solutions LLC.
Effective date
2021-12-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:19:42

Label at a glance#

ProductNeuroComfort Pain Relief
Active ingredientLIDOCAINE
Label structure6 sections

Label contents#

Full prescribing information#

For NDC 73096-021 NeuroComfort Pain Relief

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For NDC 73096-021For NDC 73096-021

For NDC 73096-022 NeuroComfort Pain Relief Gel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For NDC 73096-022For NDC 73096-022

SPL UNCLASSIFIED SECTION

For NDC 73096-022-02For NDC 73096-022-02

For NDC 73096-023 NeuroComfort Pain Relif Gel Extra Strength

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For NDC 73096-023For NDC 73096-023

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For NDC 73096-023-02For NDC 73096-023-02

For NDC 73096-024 NeuroComfort Pain Relief Roll-on

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For NDC 73096-024For NDC 73096-024

SPL UNCLASSIFIED SECTION

For NDC 73096-024-02For NDC 73096-024-02

For NDC 73096-025 NeuroComfort Pain Relief Roll-on Extra Strength

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For NDC 73096-025For NDC 73096-025

SPL UNCLASSIFIED SECTION

For NDC 73096-025-02For NDC 73096-025-02

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73096-02173096-021-01
73096-02273096-022-01, 73096-022-02
73096-02373096-023-01, 73096-023-02
73096-02473096-024-01, 73096-024-02
73096-02573096-025-01, 73096-025-02

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 70 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUNFLOWER OIL3W1JG795YIIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
EUCALYPTUS OIL2R04ONI662IACT
COMFREY LEAFDG4F8T839XIACT
DIMETHICONE 1000MCU2324216IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CAPSAICINS07O44R1ZMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
HEMPTD1MUT01Q7IACT
LIDOCAINE98PI200987ACTIB
SUNFLOWER OIL3W1JG795YIIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
COMFREY LEAFDG4F8T839XIACT
DIMETHICONE 1000MCU2324216IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CAPSAICINS07O44R1ZMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
HEMPTD1MUT01Q7IACT
EUCALYPTUS OIL2R04ONI662IACT
LIDOCAINE98PI200987ACTIB
SUNFLOWER OIL3W1JG795YIIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
COMFREY LEAFDG4F8T839XIACT
DIMETHICONE 1000MCU2324216IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CAPSAICINS07O44R1ZMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
HEMPTD1MUT01Q7IACT

Source Document#

Source XML · Source PDF

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
f1007eaa-eaeb-1b70-e053-2995a90ace0d8ded2efa-1753-7a0f-e053-2a95a90aca152022-12-29WarningsExact identifier
spl set id: 8ded2efa-1753-7a0f-e053-2a95a90aca15

Reported adverse events (FAERS/openFDA)#

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