FDA.reportPublic FDA data

PS

Manufacturer
New Leaf Pharmaceutical, LLC
Effective date
2020-01-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:30

Label at a glance#

ProductPS
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure1 sections

Label contents#

Full prescribing information#

CBD Power Salve

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Power SalvePower Salve

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71798-005-032022-01-28C16284748780-1d6a99b39-a0ae-a426-e053-dadaa90af4c2CBD Power Salve

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71798-005-03PS88.7 mg in 1 JAROINTMENT88.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71798-005PS (MENTHOL) OINTMENT [NEW LEAF PHARMACEUTICAL, LLC]1Legacy NDC, 1 package rows20200401_9cf71ce2-8b38-22eb-e053-2a95a90a0d98.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71798-00571798-005-03

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
PEPPERMINT OILAV092KU4JHIACT
BLACK PEPPER OILU17J84S19ZIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
ALOE VERA LEAFZY81Z83H0XIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
BOSWELLIA SERRATA WHOLEX7B7P649WQIACT

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
9cf71ce2-8b39-22eb-e053-2a95a90a0d989cf71ce2-8b38-22eb-e053-2a95a90a0d982020-01-25Exact identifier
spl id: 9cf71ce2-8b39-22eb-e053-2a95a90a0d98
spl set id: 9cf71ce2-8b38-22eb-e053-2a95a90a0d98

Reported adverse events (FAERS/openFDA)#

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