Shelo NABEL Gel para Golpes

Manufacturer: Corporativo Serysi S de R L de C V
Effective date: 2019-10-14
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-05-31 23:00:47

Label at a glance#

ProductShelo NABEL Gel para Golpes

Active ingredientMENTHOL, UNSPECIFIED FORM

Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

active ingredient

Inactive ingredient

INACTIVE INGREDIENT SECTION

Inactive Ingredient

warnings

WARNINGS SECTION

warnings

Uses

OTC - PURPOSE SECTION

Uses

KROC

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KROC

ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

aDMON

iNDICATIONS

INDICATIONS & USAGE SECTION

Indications

Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1923141	menthol 2.6 % Topical Gel	PSN	6
1923141	menthol 0.026 MG/MG Topical Gel	SCD	6
1923141	menthol 2.6 % Topical Gel	SY	6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71424-1347-1	2021-01-29	C162847	48780-1	ba0f9c33-1fdc-a910-e053-dadaa90a0b85	Sheló NABEL Gel Para Golpes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71424-1347-1	Shelo NABEL Gel para Golpes	260 g in 1 BOTTLE	GEL	260		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71424-1347	SHELO NABEL GEL PARA GOLPES (MENTHOL) GEL [CORPORATIVO SERYSI S DE R L DE C V]	6	Legacy NDC, 1 package rows	20191015_5038bc96-95d0-7419-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Shelo NABEL Gel para Golpes
Menthol
MENTHOL, UNSPECIFIED FORM
MINT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71424-1347	71424-1347-1

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
Name	UNII	Kind
MENTHOL, UNSPECIFIED FORM	L7T10EIP3A	ACTIB
MINT	FV98Z8GITP	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
94e9a33f-39c6-4bc5-e053-2a95a90a43ac			5038bc96-95d0-7419-e054-00144ff88e88	2019-10-14	Warnings	Exact identifier spl id: 94e9a33f-39c6-4bc5-e053-2a95a90a43ac spl set id: 5038bc96-95d0-7419-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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