dermaFIT Muscle Retention Cream Sculpt

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]

DERMAFIT MUSCLE RETENTION CREAM SCULPT- menthol cream 
EX Healthcare Inc.

----------

dermaFIT Muscle Retention Cream Sculpt

MENTHOL 0.1%

Topical Analgesic

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.

For external use only.

to wounds or damaged skin.

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

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

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.

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

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.

primarybox

DERMAFIT MUSCLE RETENTION CREAM SCULPT 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 82679-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.1 g  in 200 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
AQUA (UNII: 059QF0KO0R)  
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
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 82679-103-021 in 1 BOX09/14/202512/17/2025
1NDC: 82679-103-01200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/14/202512/17/2025
Labeler - EX Healthcare Inc. (695315496)
Establishment
NameAddressID/FEIBusiness Operations
EX Healthcare Inc.695315496label(82679-103)
Establishment
NameAddressID/FEIBusiness Operations
Kolmar Korea Co.,Ltd963271745manufacture(82679-103)

Revised: 12/2025
 

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.