FDA.reportPublic FDA data

CBD Power Spray Professional

Manufacturer
New Leaf Pharmaceutical, LLC | New Leaf Pharmaceuticals, LLC
Effective date
2019-10-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:51

Label at a glance#

ProductProf
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure1 sections

Label contents#

Full prescribing information#

CBD Power Spray Professional

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CBD Power Spray ProfCBD Power Spray Prof

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71798-004-032021-01-29C16284748780-1ba0f9c33-3369-a910-e053-dadaa90a0b85CBD Power Spray Professional

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71798-004-03Prof88.7 mL in 1 CANSPRAY88.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71798-004PROF (MENTHOLXS) SPRAY [NEW LEAF PHARMACEUTICAL, LLC]1Legacy NDC, 1 package rows20191017_9508ff4c-b08d-e207-e053-2a95a90a200a.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71798-00471798-004-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CAPSICUM ANNUUM WHOLE7FKZ3QQQ1FIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WILLOW BARKS883J9JDYXIACT
PEPPERMINT OILAV092KU4JHIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
CANNABIDIOL19GBJ60SN5IACT
EMU OIL344821WD61IACT
METHYL SALICYLATELAV5U5022YIACT

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
9508ff4c-b08e-e207-e053-2a95a90a200a9508ff4c-b08d-e207-e053-2a95a90a200a2019-10-16Exact identifier
spl id: 9508ff4c-b08e-e207-e053-2a95a90a200a
spl set id: 9508ff4c-b08d-e207-e053-2a95a90a200a

Reported adverse events (FAERS/openFDA)#

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