Sheló NABEL Pomada Árnica Gel

Manufacturer
Corporativo Serysi S de R L de C V
Effective date
2019-10-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:00:50

Label at a glance#

ProductShelo NABEL Pomada Arnica
Active ingredientMENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC)
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient U059

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient U059Active Ingredient U059

Inactive Ingredient U059

INACTIVE INGREDIENT SECTION

Inactive Ingredient U059Inactive Ingredient U059

Warnings U059

WARNINGS SECTION

Warnings U059Warnings U059

Uses U059

OTC - PURPOSE SECTION

Uses U059Uses U059

KROC U059

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KROC U059KROC U059

Administration U059

DOSAGE & ADMINISTRATION SECTION

Admon U059Admon U059

Indications U059

INDICATIONS & USAGE SECTION

Indications U059Indications U059

Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Display Panel U059Display Panel U059

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1923414camphor 3 % / menthol 2 % Topical GelPSN4
1923414camphor 0.03 MG/MG / menthol 0.02 MG/MG Topical GelSCD4
1923414camphor 3 % / menthol 2 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71424-1059-12021-01-29C16284748780-1ba0f9c33-5bcb-a910-e053-dadaa90a0b85Sheló NABEL Pomada Árnica Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71424-1059-1Shelo NABEL Pomada Arnica140 g in 1 BOTTLE, DISPENSINGGEL1404

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71424-1059SHELO NABEL POMADA ARNICA (MENTHOL) GEL [CORPORATIVO SERYSI S DE R L DE C V]4Legacy NDC, 1 package rows20191016_5034e943-d90d-56d3-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71424-105971424-1059-1

Ingredients#

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

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

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
94faccff-9c08-ac28-e053-2a95a90ac7265034e943-d90d-56d3-e054-00144ff8d46c2019-10-15WarningsExact identifier
spl id: 94faccff-9c08-ac28-e053-2a95a90ac726
spl set id: 5034e943-d90d-56d3-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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