DERMAFIT MUSCLE RETENTION CREAM SCULPT- menthol cream

dermaFIT Muscle Retention Cream Sculpt by

Drug Labeling and Warnings

dermaFIT Muscle Retention Cream Sculpt by is a Otc medication manufactured, distributed, or labeled by EX Healthcare Inc., Kolmar Korea Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

MENTHOL 0.1%

PURPOSE

Topical Analgesic

INDICATIONS & USAGE

For the recovery of muscle post workout and the
temporary relief of minor aches and pains of muscles and
joints associated with sprains, arthritis, and strains.

WARNINGS

For external use only.

DO NOT USE

to wounds or damaged skin.

WHEN USING

When using this product avoid contact with eyes and
mucous membranes.

STOP USE

if condition worsens, symptoms
persist for more than 7 days or clear up and occur again
within a few days.

KEEP OUT OF REACH OF CHILDREN

If product is swallowed, get
medical help or contact a Poison Control Center right away.
If pregnant or breast-feeding, ask a health professional
before use.

INACTIVE INGREDIENT

Water, Propanediol, Glycerin, Butylene Glycol, Cetyl
Ethylhexanoate, 1,2-Hexanediol, Camellia Japonica Flower
Extract, Sorbitan Olivate, Cetearyl Glucoside, Cetearyl
Olivate, Betaine, Arginine, Sodium Hyaluronate, Carbomer,
Silica, Ethylhexylglycerin, Cetearyl Alcohol

OTHER SAFETY INFORMATION

Store at room temperature.

Directions

Apply to affected area not more than 3 to 4 times daily.
Children under 12 years of age: consult a doctor.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMAFIT MUSCLE RETENTION CREAM SCULPT 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82679-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.1 g  in 200 mL

Inactive Ingredients
Ingredient Name	Strength
AQUA (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PROPANEDIOL (UNII: 5965N8W85T)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
SILICA (UNII: ETJ7Z6XBU4)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CARBOMER (UNII: 0A5MM307FC)
ARGININE (UNII: 94ZLA3W45F)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
BETAINE (UNII: 3SCV180C9W)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
MENADIONE (UNII: 723JX6CXY5)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
CENTELLA ASIATICA LEAF (UNII: 6810070TYD)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82679-103-02	1 in 1 BOX	09/14/2025
1	NDC: 82679-103-01	200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/14/2025

Labeler - EX Healthcare Inc. (695315496)

Establishment
Name	Address	ID/FEI	Business Operations
EX Healthcare Inc.		695315496	label(82679-103)

Establishment
Name	Address	ID/FEI	Business Operations
Kolmar Korea Co.,Ltd		963271745	manufacture(82679-103)