Sheló NABEL Hielo Mineral Topical Analgesic Spray

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 Hielo Mineral
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM
Label structure8 sections

Label contents#

Full prescribing information#

Actieve Ingredient U060

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient U060Active Ingredient U060

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Inactive U060Inactive U060

Warnings

WARNINGS SECTION

Warnings U060Warnings U060

KROC U060

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KROCK U060KROCK U060

Uses U060

OTC - PURPOSE SECTION

Uses U060Uses U060

Administration

DOSAGE & ADMINISTRATION SECTION

Administration U060Administration U060

Indications U060

INDICATIONS & USAGE SECTION

Indications U060Indications U060

Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Display Panel U060Display Panel U060

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1923699camphor 0.2 % / menthol 1.25 % Topical SprayPSN4
1923699camphor 2 MG/ML / menthol 12.5 MG/ML Topical SpraySCD4
1923699camphor 0.2 % / menthol 1.25 % Topical SpraySY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71424-1060-12021-01-29C16284748780-1ba0f9c33-478b-a910-e053-dadaa90a0b85Sheló NABEL Hielo Mineral Topical Analgesic Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71424-1060-1Shelo NABEL Hielo Mineral260 g in 1 BOTTLE, SPRAYSPRAY2604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71424-1060SHELO NABEL HIELO MINERAL (MENTHOL) SPRAY [CORPORATIVO SERYSI S DE R L DE C V]4Legacy NDC, 1 package rows20191016_5020a7e1-65a9-53f0-e054-00144ff88e88.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
71424-106071424-1060-1

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 · 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
94fa4adb-66a7-905e-e053-2995a90a3da35020a7e1-65a9-53f0-e054-00144ff88e882019-10-15WarningsExact identifier
spl id: 94fa4adb-66a7-905e-e053-2995a90a3da3
spl set id: 5020a7e1-65a9-53f0-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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