FDA.reportPublic FDA data

XCEPTOR CBD PAIN CREAM - MENTHOL

Manufacturer
XCEPTOR LLC
Effective date
2020-07-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:21:30

Label at a glance#

ProductXCEPTOR CBD PAIN MENTHOL
Active ingredientMETHYL SALICYLATE
Label structure10 sections

Indications and uses

TOPICAL PAIN RELIEF FOR MINOR ACHES AND PAINS.

Dosage and administration

APPLY SMALL AMOUNT TO AFFECTED AREA AND RUB IN. ADD AS NEEDED.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

METHYL SALICYLATE  10%

PURPOSE

OTC - PURPOSE SECTION

TOPICAL ANALGESIC

USES

INDICATIONS & USAGE SECTION

TOPICAL PAIN RELIEF FOR MINOR ACHES AND PAINS.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

KEEP AWAY FROM EYES.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY SMALL AMOUNT TO AFFECTED AREA AND RUB IN. ADD AS NEEDED.

OTHER INFORMATION

OTHER SAFETY INFORMATION

STORE AT 20° - 25°C (68°-77°F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ALOE BARBADENSIS LEAF JUICE EXTRACT, BENZOIC ACID, BENZYL ALCOHOL, BETA VULGARIS (BEET) ROOT EXTRACT, CANNABIDIOL FROM HEMP, COCOCAPRYLATE/CAPRATE, COCOS NUCIFERA (COCONUT) OIL, COCONUT ALKANES, CYCLODEXTRIN, DISTEARDIMONIUM HECTORITE, GLYCERIN, MAGNESIUM SULFATE, POLYGLYCERYL-3 DIISOSTEARATE, POLYGLYCERYL-3 POLYRICINOLEATE, SHEA BUTTER ETHYL ESTERS, SORBIC ACID, TREMELLA FUCIFORMIS SPOROCARP EXTRACT, XANTHAN GUM, WATER

QUESTIONS / COMMENTS?

OTC - QUESTIONS SECTION

PLEASE CALL US AT (760) 710-0510

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Xceptor_CBD Pain Cream_Menthol_LBLXceptor_CBD Pain Cream_Menthol_LBL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72519-104-212022-01-28C16284748780-1d6a99b39-5d0d-a426-e053-dadaa90af4c2XCEPTOR CBD PAIN CREAM - MENTHOL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72519-104-21XCEPTOR CBD PAINMENTHOL30 mL in 1 BOTTLE, DISPENSINGCREAM304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72519-104XCEPTOR CBD PAIN MENTHOL (METHYL SALICYLATE) CREAM [XCEPTOR LLC]4Legacy NDC, 1 package rows20200716_6df8f8bb-30e3-4d82-8c7b-a82fa74b4c37.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72519-10472519-104-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYL SALICYLATELAV5U5022YACTIB
ALOE VERA LEAFZY81Z83H0XIACT
BENZOIC ACID8SKN0B0MIMIACT
BENZYL ALCOHOLLKG8494WBHIACT
BEETN487KM8COKIACT
CANNABIDIOL19GBJ60SN5IACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
COCONUT OILQ9L0O73W7LIACT
COCONUT ALKANES1E5KJY107TIACT
BETADEXJV039JZZ3AIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
GLYCERINPDC6A3C0OXIACT
MAGNESIUM SULFATE ANHYDROUSML30MJ2U7IIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
SHEA BUTTER ETHYL ESTERSV2CI786FPGIACT
SORBIC ACIDX045WJ989BIACT
TREMELLA FUCIFORMIS FRUITING BODYGG8N28393GIACT
XANTHAN GUMTTV12P4NEEIACT
WATER059QF0KO0RIACT

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
15fd2c61-fbc9-4761-9270-8e14c5d23fbd6df8f8bb-30e3-4d82-8c7b-a82fa74b4c372020-07-15WarningsExact identifier
spl id: 15fd2c61-fbc9-4761-9270-8e14c5d23fbd
spl set id: 6df8f8bb-30e3-4d82-8c7b-a82fa74b4c37

Reported adverse events (FAERS/openFDA)#

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