ProCBD Pain Cream (Muscle) 4oz

Manufacturer
CV Sciences, Inc. | Filltech USA, LLC
Effective date
2021-08-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:38:00

Label at a glance#

ProductProCBD Pain Cream (Muscle) 4oz
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure9 sections

Indications and uses

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

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 5%

Menthol 4%

Purpose

OTC - PURPOSE SECTION

Camphor 5%..........................Topical Analgesic

Menthol 4%............................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

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, isopropyl alcohol, glycerin, cetearyl olivate, sorbitan olivate, cannabidiol, phenoxyethanol, aloe barbadensis leaf juice, xanthan gum, isopropyl myristate, lysolecitihin, sclerotium gum, pullulan, arnica montana extract, calendula officinalis flower extract, tocopheryl acetate, carthamus tinctorius (safflower) seed oil, salix alba (willow) bark extract, symphytum officinale (comfrey) extract, citric acid

Questions?

OTC - QUESTIONS SECTION

855-758-7223

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

+ProCBD

Pain Relief

Level 1

Muscle Cream

Temporary Pain Relief for:

Strains

Backache

Neckache

Camphor 5% | Menthol 4%

Pain Relieving Cream

Net wt. 4 oz (113.4 g)

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82026-61482026-614-62

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
290614ef-c345-05b4-e063-6294a90ad39cca3a33ea-ce54-c209-e053-2995a90abe202024-12-11WarningsExact identifier
spl set id: ca3a33ea-ce54-c209-e053-2995a90abe20

Reported adverse events (FAERS/openFDA)#

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