FDA.reportPublic FDA data

HEMP THE POINT

Manufacturer
Lab-Clean, Inc | LAB-CLEAN, LLC
Effective date
2022-04-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:02:34

Label at a glance#

ProductHEMP THE POINT
Active ingredientEUCALYPTUS GUM, MENTHOL
Label structure6 sections

Indications and uses

Helps relax and recover tensed-up or sore muscles post-workout / also ideal for general daily use for therapeutic relief on the body / the combination of active ingredients helps soothe and moisturize the skin.

Dosage and administration

SHAKE WELL BEFORE USE Apply as needed on the affected area to relieve muscle tension. Rub with hand post application to help product seep into skin. Ideal for daily use

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS                                                        PURPOSE

OTC - ACTIVE INGREDIENT SECTION

Eucalyptus Globulus                                                             Cooling Relief

Menthol                                                                               Muscle Recovery

USES

INDICATIONS & USAGE SECTION

Helps relax and recover tensed-up or sore muscles post-workout / also ideal for general daily use for therapeutic relief on the body / the combination of active ingredients helps soothe and moisturize the skin.

DIRECTIONS

OTC - PURPOSE SECTION

SHAKE WELL BEFORE USE

Apply as needed on the affected area to relieve muscle tension. Rub with hand post application to help product seep into skin. Ideal for daily use

WARNINGS

WARNINGS SECTION

External use only / KEEP OUT OF REACH OF CHILDREN / Ask a doctor prior to use if you: have sensitive skin, are pregnant or breast
feeding, or plan to use on children <2 years old / Do not get in eyes, wounds or damaged skin / Stop immediately if condition worsens and
consult with doctor.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water 7732-18-5, Sunflower Oil 8001-21-6, Glycerine 56-81-5, Hemp Seed Oil 8016-24-8,
Emulsifier 3055-97-8, Phenoxyethanol, Ethylhexylglycerine 122-99-6 and 70445-33-9.

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73126-00173126-001-01

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
SUNFLOWER OIL3W1JG795YIIACT
GLYCERINPDC6A3C0OXIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EUCALYPTUS GUM72T9EZC2VXACTIB
MENTHOLL7T10EIP3AACTIB

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
dd93bd82-d52e-2136-e053-2a95a90afe7ad7963f9a-1947-45c0-974d-dab7cf4720cf2022-04-26WarningsExact identifier
spl id: dd93bd82-d52e-2136-e053-2a95a90afe7a
spl set id: d7963f9a-1947-45c0-974d-dab7cf4720cf

Reported adverse events (FAERS/openFDA)#

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