MYCO CLINIC PAIN RELIEF- menthol cream

MYCO Clinic Pain Relief by

Drug Labeling and Warnings

MYCO Clinic Pain Relief by is a Otc medication manufactured, distributed, or labeled by Aidance Skincare & Topical Solutions, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients                Purpose

Menthol USP, 4%..........Topical analgesic

PURPOSE

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 breastfeeding, ask a health professional before use.

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

KEEP OUT OF REACH OF CHILDREN

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

Arnica Extract, Colloidal Oatmeal, Ginger Extract, Honeysuckle Oil, Jojoba Oil, MCT/Coconut Oil, Mushroom Extracts - USDA Organic (Cordyceps, Lion's Mane, Reishi, Shiitake), Purified Water, Shea Butter, Sorbic Acid, Sunflower Oil, Sweet Orange Oil, Turmeric Extract, Camphor, Emulsifying Wax

Questions?

myco-clinic.com
Questions? 401-671-6170

Product label

INGREDIENTS AND APPEARANCE

MYCO CLINIC PAIN RELIEF 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24909-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
OATMEAL (UNII: 8PI54V663Y)
GINGER (UNII: C5529G5JPQ)
AQUILEGIA CANADENSIS WHOLE (UNII: 636VYW51FP)
JOJOBA OIL (UNII: 724GKU717M)
COCONUT OIL (UNII: Q9L0O73W7L)
CULTIVATED MUSHROOM (UNII: 54C8E6W6JY)
OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU)
REISHI (UNII: TKD8LH0X2Z)
SHIITAKE MUSHROOM (UNII: 1A64QN2D2F)
WATER (UNII: 059QF0KO0R)
SHEA BUTTER (UNII: K49155WL9Y)
SORBIC ACID (UNII: X045WJ989B)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)
TURMERIC (UNII: 856YO1Z64F)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
HERICIUM ERINACEUS FRUITING BODY (UNII: BU6Y4J4C2E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24909-010-50	50 g in 1 TUBE; Type 0: Not a Combination Product	02/24/2023
2	NDC: 24909-010-20	200 g in 1 TUBE; Type 0: Not a Combination Product	02/24/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/24/2023

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

Establishment
Name	Address	ID/FEI	Business Operations
Aidance Skincare & Topical Solutions, LLC		018950611	manufacture(24909-010)