Label: MYDERM COOLING MENTHOL PAIN RELIEF WITH 50 PERCENT MORE MENTHOL- menthol spray
- NDC Code(s): 72667-020-01
- Packager: Inspec Solutions LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 10, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
-
INACTIVE INGREDIENT
INACTIVE INGREDIENTS
Aloe Barbadensis Leaf Extract
Arctium Lappa Root (Burdock) Extract
Arnica Montana Flower Extract
Boswellia Carterii Resin Extract
Calendula Officinalis Extract
Camellia Sinensis Leaf Extract
Camphor
Carbomer
FD&C Blue #1
FD&C Yellow #5
Full Spectrum Industrial Hemp Extract
Glycerin
Ilex Paraguariensis (Mate) Leaf Extract
Isopropyl Alcohol
Isopropyl Myristate
Melissa Officinalis (Lemon Balm) Leaf Extract
Silica
Tocopheryl Acetate
Triethanolamine
Water
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MYDERM COOLING MENTHOL PAIN RELIEF WITH 50 PERCENT MORE MENTHOL
menthol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72667-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 15.75 g in 100 mL Inactive Ingredients Ingredient Name Strength FRANKINCENSE (UNII: R9XLF1R1WM) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) GLYCERIN (UNII: PDC6A3C0OX) MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CAMPHOR (NATURAL) (UNII: N20HL7Q941) CARBOMER 940 (UNII: 4Q93RCW27E) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ISOPROPYL ALCOHOL (UNII: ND2M416302) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72667-020-01 89 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/27/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 12/27/2021 Labeler - Inspec Solutions LLC (081030372) Establishment Name Address ID/FEI Business Operations Inspec Solutions LLC. 081030372 manufacture(72667-020)