GREEN LEAF CBD ULTRA RELIEF

Manufacturer
SURF LINE, INC
Effective date
2024-11-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:48:48

Label at a glance#

ProductGREEN LEAF CBD ULTRA RELIEF
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure11 sections

Indications and uses

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

Dosage and administration

Adults and Children over 12 years: Apply a small amount on the area to be. Massage in circular motion until absorbed. Repeat as needed, but no more than 3 to 4 times per day. Store tightly closed in a dry place at room temperature between 59°-86° F (15°-30° C). Wash hands with soap and water after use.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 6%

Camphor 2%

OTC - PURPOSE SECTION

Topical Analgesic.

Pain Relieving.

USES:

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Use only as directed.
Do not bandage tightly or use with a heating pad.
Avoid contact with eyes and mucous membranes.
Do not apply to wounds or damaged, broken, or irritated skin.
A transient burning sensation or redness may occur upon application but generally disappears in several days.
If you experience an allergic reaction, discontinue use, and consult a doctor.

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

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.

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.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years:

Apply a small amount on the area to be.
Massage in circular motion until absorbed.
Repeat as needed, but no more than 3 to 4 times per day.
Store tightly closed in a dry place at room temperature between 59°-86° F (15°-30° C).

Wash hands with soap and water after use.

INACTIVE INGREDIENT SECTION

Aqua, Alcohol Denat, Propylene Glycol, Polysorbate 20, Salicylic Acid, Glycerin, Carbomer, Sodium Hydroxide, Mentha Arvensis Herb Oil, Cannabidiol, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Delta-8-Tetrahydrocannabinol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Benzyl Alcohol, Sorbic Acid, FD&C Blue. 1 Powder (CI 42090), FD&C Yellow. 5 (CI 19140), Limonene.

GREEN LEAF CBD ULTRA RELIEF GEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GREEN LEAF RELIEF GELGREEN LEAF RELIEF GEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83345-602GREEN LEAF CBD ULTRA RELIEF (MENTHOL, CAMPHOR) GEL [SURF LINE, INC]3Unmatched20241124_f8329406-9c6f-ef63-e053-6394a90a1d20.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83345-60283345-602-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
4461c0a7-f4fb-65c7-e063-6394a90a8bfcf8329406-9c6f-ef63-e053-6394a90a1d202025-11-24WarningsExact identifier
spl set id: f8329406-9c6f-ef63-e053-6394a90a1d20

Reported adverse events (FAERS/openFDA)#

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