FDA.reportPublic FDA data

SinolM™ Fast Headache Pain Relief All-Natural Nasal Spray

Manufacturer
Sinol USA, Inc.
Effective date
2025-01-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:53:55

Label at a glance#

ProductSinolM Fast Headache Pain Relief All-Natural
Active ingredientCAPSICUM
Label structure1 sections

Label contents#

Full prescribing information#

PRINCIPAL DISPLAY PANEL - 15 ml Bottle Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FAST RELIEF
HEADACHE

NEW
FORMULA

Sinol m™

All-Natural
Nasal Spray
HEADACHE

15 ml

PRINCIPAL DISPLAY PANEL - 15 ml Bottle Box
PRINCIPAL DISPLAY PANEL - 15 ml Bottle Box

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAPSICUM Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
15013-001-172023-02-10C16284748780-1f386c649-b6a6-0266-e053-dadaa90a7c1aSinolM™ Fast Headache Pain Relief All-Natural Nasal Spray
15013-001-172023-01-30C16284748780-1f386c649-b6a6-0266-e053-dadaa90a7c1aSinolM™ Fast Headache Pain Relief All-Natural Nasal Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15013-001-17SinolM Fast Headache Pain Relief All-Natural15 mL in 1 BOTTLE, SPRAYSPRAY153

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15013-001SINOLM FAST HEADACHE PAIN RELIEF ALL-NATURAL (CAPSICUM) SPRAY [SINOL USA, INC.]31 package rows20250130_6bb74d41-e14b-4523-9950-46ab41466898.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
15013-00115013-001-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SILVER3M4G523W1GIACT
ALOEV5VD430YW9IACT
EUCALYPTOLRV6J6604TKIACT
ROSEMARYIJ67X351P9IACT
SEA SALT87GE52P74GIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
CAPSICUM00UK7646FGACTIB

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
2cddd967-0e57-21f1-e063-6394a90a7e5d6bb74d41-e14b-4523-9950-46ab414668982025-01-29Exact identifier
spl id: 2cddd967-0e57-21f1-e063-6394a90a7e5d
spl set id: 6bb74d41-e14b-4523-9950-46ab41466898

Reported adverse events (FAERS/openFDA)#

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