PlusCBD Pain Cream (Arthritis) 2oz

Manufacturer
CV Sciences, Inc. | Filltech USA, LLC
Effective date
2022-01-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:10:20

Label at a glance#

ProductPlusCBD Pain Cream (Arthritis) 2oz
Active ingredientCAMPHOR (NATURAL), MENTHOL
Label structure9 sections

Indications and uses

temporarily relieves minor aches and pains of muscles and joints associated with: arthritis strains sprains bruises

Dosage and administration

apply thin layer and gently massage until it disappears after applying, wash hands with soap and water adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily children under 12 years of age: consult a physician

Storage and handling

store in cool dry place, away from direct sunlight

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 10%

Menthol 5%

Purpose

OTC - PURPOSE SECTION

Camphor 10%.........Topical Analgesic

Menthol 5%.............Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves minor aches and pains of muscles and joints associated with:
  • arthritis
  • strains
  • sprains
  • bruises

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin
  • on irritated skin

OTC - WHEN USING SECTION

When using this product

  • avoid contact with the eyes and mucous membranes
  • do not bandage tightly or use with a heating pad

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • you experience swelling or blistering of the skin

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply thin layer and gently massage until it disappears
  • after applying, wash hands with soap and water
  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age: consult a physician

Other information

STORAGE AND HANDLING SECTION

store in cool dry place, away from direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, caprylic/capric triglyceride, cetearyl olivate, stearic acid, glycerin, sorbitan olivate, cetyl alcohol, cannabidiol, sclerocarya birrea (marula) seed oil, argania spinosa kernel oil, eucalyptus globulus leaf oil, phenoxyethanol, xanthan gum, boswellia carterii (frankincense) oil, lavandula angustifolia (lavender) oil, ethylhexylglycerin

Questions?

OTC - QUESTIONS SECTION

855-758-7223

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

+PlusCBD

Pain Relief

Arthritis Cream

Temporary Pain Relief for:

Joints

Hands

Feet

Camphor 10% Menthol 5%

Pain Relieving Cream

Net wt. 2 oz (56.7 g)

11

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82026-61082026-610-59

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
29060c13-4ccf-482b-e063-6294a90a760dca398dfb-81f8-eee3-e053-2995a90ab1f72024-12-11WarningsExact identifier
spl set id: ca398dfb-81f8-eee3-e053-2995a90ab1f7

Reported adverse events (FAERS/openFDA)#

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