CBD CLINIC DEEP-RUB PAIN RELIEF - LEVEL 5- camphor, menthol oil

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredients

Camphor USP, 5%, Menthol USP, 15%

Purpose

Camphor, Menthol - Topical Analgesics

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
Wash hands with soap and water after use (unless applying to hands)
children under 12 years of age: ask a doctor

Inactive Ingredients

CBD hemp oil, cottonseed oil, jojoba seed oil

Questions?

Call 1-888-422-3254

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CBD CLINIC DEEP-RUB PAIN RELIEF - LEVEL 5 
camphor, menthol oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24909-754
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	5 g  in 100 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COTTONSEED OIL (UNII: H3E878020N)
HEMP (UNII: TD1MUT01Q7)
JOJOBA OIL (UNII: 724GKU717M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24909-754-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2019
2	NDC: 24909-754-28	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2019
3	NDC: 24909-754-64	1893 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/15/2019

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

Establishment
Name	Address	ID/FEI	Business Operations
Aidance Skincare & Topical Solutions, LLC		018950611	manufacture(24909-754) , label(24909-754)