JUST CBD ULTRA RELIEF

Manufacturer
Just Brands LLC
Effective date
2025-11-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:17:29

Label at a glance#

ProductJUST CBD ULTRA RELIEF
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure14 sections

Dosage and administration

Adults over 21 years: Apply a small amount to the affected area. Massage in circular motion until absorbed. Repeat as needed, but no more than 3 to 4 times per day. Wash hands with soap and water after use.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Camphor 2%

Menthol 6%

OTC - PURPOSE SECTION

Topical Analgesic

USE

INDICATIONS & USAGE SECTION

Aid for temporary local relief of minor pain in muscles or joints.

WARNINGS SECTION

For external use only.

OTC - ASK DOCTOR SECTION

Ask a doctore before use if you have redness over affected area

OTC - WHEN USING SECTION

Use only as directed.
Do not bandage tightly

Do not use with heating pad, pack, wrap hot water bottle or any heating element.
Avoid contact with eyes.
Do not apply to wounds or damaged, broken, or irritated skin.

Do not expose the area treated with product to heat or direct sunlight.

STOP USE AND ASK A DOCTOR IF:

OTC - STOP USE SECTION

Condition worsens.
Redness is present.
Irritation develops.
Symptoms persist for more than 7 days or clear up occur again within a few days.

You experience signs injury, such as pain, swelling or blistering where the product was applied.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults over 21 years:

Apply a small amount to the affected area.
Massage in circular motion until absorbed.
Repeat as needed, but no more than 3 to 4 times per day.

Wash hands with soap and water after use.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Store tightly closed in a dry place at controlled temperature between 59°-86° F (15°-30° C).

This product is intended only for use by healthy adults aged 21 years & older.

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Alcohol Denat, Polysorbate 20, Mentha Piperita (Peppermint) Oil, Cannabidiol, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Carbomer, Sodium Hydroxide, Benzyl Alcohol, Salicylic Acid, Glycerin, Sorbic Acid, FD&C Blue. 1 Powder (CI 42090), FD&C Yellow. 5 (CI 19140), Limonene.

JUST CBD ULTRA RELIEF GEL +1000

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ultra relief 1000ultra relief 1000

JUST CBD ULTRA RELIEF GEL +5000

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ultra relief 5000ultra relief 5000

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130696831876794GTIN-13: 0696831876794
EAN-13: 0696831876794
GTIN-12: 696831876794
UPC-A: 696831876794
GTIN storage (14 digits): 00696831876794
FD-04267 JUST CBD - ULTRA RELIEF GEL 1000 CBD VER 2 73647-602-04.jpg
QR code linkQR Codewww.justcbdstore.com/lab-reports/FD-04268 JUST CBD - ULTRA RELIEF GEL 5000 CBD VER 2 73647-206-04.jpg, FD-04267 JUST CBD - ULTRA RELIEF GEL 1000 CBD VER 2 73647-602-04.jpg

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73647-206-04JUST CBD ULTRA RELIEF118 mL in 1 BOTTLE, PUMPGEL1183
73647-602-04JUST CBD ULTRA RELIEF118 mL in 1 BOTTLE, PUMPGEL1183

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
73647-20673647-206-04
73647-60273647-602-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 40 matching rows.

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
43d6b434-3f26-f948-e063-6294a90ad22ef65327b3-9c97-58f3-e053-2995a90a3f552025-11-17WarningsExact identifier
spl id: 43d6b434-3f26-f948-e063-6294a90ad22e
spl set id: f65327b3-9c97-58f3-e053-2995a90a3f55

Reported adverse events (FAERS/openFDA)#

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