CBD-BEE-DOO Arthritis Relief Cream

CBD BEE DOO Arthritis Relief by

Drug Labeling and Warnings

CBD BEE DOO Arthritis Relief by is a Otc medication manufactured, distributed, or labeled by Diesel-stilfen, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CBD BEE DOO ARTHRITIS RELIEF- camphor (synthetic), menthol cream 
Diesel-stilfen, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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CBD-BEE-DOO Arthritis Relief Cream

Drug Facts

Active Ingredient:

Camphor 11%, Menthol 16%

Purpose

Topical Analgesic

Use

• Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Warnings:

For external use only.

Do not use

on wounds

• damaged skin
• with a heating pad or bandage tightly.

When using this product

avoid contact with eyes or mucous membranes. 

Stop use and ask a doctor if

• condition worsens or symptoms persist more than 7 days
• symptoms clear and occur again with a few days
• excessive skin irritation develops.

Keep out of reach of children.

If pregnant or breast-feeding,

ask a health professional before use. If swallowed, get medical help or contact a poison control center immediately.

Additional information:

Store at room temperature

Directions:

Adults and children 12 years of age and older: apply to affected area no more than 3 to 4 times daily. Children under 12 years of age: Ask a doctor.

Inactive ingredients:

Beeswax, hemp extract, isopropyl myristate, olive oil

Package Labeling:

CBD BEE DOO ARTHRITIS RELIEF 
camphor (synthetic), menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79220-164
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	110 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	160 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
YELLOW WAX (UNII: 2ZA36H0S2V)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
OLIVE OIL (UNII: 6UYK2W1W1E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79220-164-45	45 g in 1 JAR; Type 0: Not a Combination Product	06/25/2020	09/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/25/2020	09/30/2022

Labeler - Diesel-stilfen, LLC (117515993)

Revised: 1/2022

Document Id: d58d3e53-208f-b9c6-e053-2a95a90a3313

34390-5

Set id: 1c21cb0a-730e-4ec0-a103-f6f70602f341

Version: 3

Effective Time: 20220114