Shelo NABEL Vibora de Cascabel Topical Analgesic Gel 250 ml

Manufacturer
Corporativo Serysi S de R L de C V
Effective date
2019-10-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:00:49

Label at a glance#

ProductShelo NABEL Vibora de Cascabel Topical Analgesic Gel 250 ml
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Warnings

WARNINGS SECTION

WarningsWarnings

Purpose

OTC - PURPOSE SECTION

PurposePurpose

KOROC

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KOROCKOROC

Administracion

DOSAGE & ADMINISTRATION SECTION

AdministrationAdministration

Indications & Usage

INDICATIONS & USAGE SECTION

IndicationsIndications

Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Display PanelDisplay Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1923141menthol 2.6 % Topical GelPSN5
1923141menthol 0.026 MG/MG Topical GelSCD5
1923141menthol 2.6 % Topical GelSY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71424-1070-12021-01-29C16284748780-1ba0f9c33-477f-a910-e053-dadaa90a0b85Sheló NABEL Víbora de Cascabel Topical Analgesic Gel 250 Ml.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71424-1070-1Shelo NABEL Vibora de Cascabel Topical Analgesic Gel 250 ml250 g in 1 BOTTLE, DISPENSINGGEL2505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71424-1070SHELO NABEL VIBORA DE CASCABEL TOPICAL ANALGESIC GEL 250 ML (MENTHOL) GEL [CORPORATIVO SERYSI S DE R L DE C V]5Legacy NDC, 1 package rows20191016_4fe37efa-9fa5-4f03-e054-00144ff8d46c.zip

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
71424-107071424-1070-1

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
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
POLYSORBATE 207T1F30V5YHIACT

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
94fac434-24e1-c246-e053-2995a90a38164fe37efa-9fa5-4f03-e054-00144ff8d46c2019-10-15WarningsExact identifier
spl id: 94fac434-24e1-c246-e053-2995a90a3816
spl set id: 4fe37efa-9fa5-4f03-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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