CBD CLINIC PAIN RELIEF - LEVEL 5- menthol, camphor stick

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredients

Menthol USP, 16%, Camphor USP, 11%

Purpose

Menthol, Camphor - Topical Analgesic

Uses

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

Warnings

For external use only
Do not use on
wounds or damaged skin
When using this product
avoid contact with eyes or mucous membranes
do not bandage tightly or use with a heating pad
Stop use and ask a doctor if
condition worsens
symptoms persist for more than 7 days
symptoms clear up and occur again within a few days
excessive skin irritation develops
If pregnant or breast-feeding
ask a health professional before use
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center immediately 

Directions

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: ask a doctor

Inactive Ingredients

beeswax, CBD hemp oil, clove oil, cottonseed oil, eucalyptus oil, jojoba seed oil, peppermint oil, shea butter, sorbic acid, tea tree oil

Questions?

Call 1-888-422-3254

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CBD CLINIC PAIN RELIEF - LEVEL 5 
menthol, camphor stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24909-766
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	16 g  in 100 g
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	11 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CLOVE OIL (UNII: 578389D6D0)
COTTONSEED OIL (UNII: H3E878020N)
EUCALYPTUS OIL (UNII: 2R04ONI662)
HEMP (UNII: TD1MUT01Q7)
JOJOBA OIL (UNII: 724GKU717M)
PEPPERMINT OIL (UNII: AV092KU4JH)
SHEA BUTTER (UNII: K49155WL9Y)
SORBIC ACID (UNII: X045WJ989B)
TEA TREE OIL (UNII: VIF565UC2G)
WHITE WAX (UNII: 7G1J5DA97F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24909-766-40	40 g in 1 CYLINDER; Type 0: Not a Combination Product	10/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/01/2019

Labeler - Aidance Skincare & Topical Solutions, LLC (018950611)

Establishment
Name	Address	ID/FEI	Business Operations
Aidance Skincare & Topical Solutions, LLC		018950611	manufacture(24909-766) , label(24909-766)