Label: METHYL SALICYLATE 25% PAIN RELIEVING- methyl salicylate cream
- NDC Code(s): 59088-014-06
- Packager: Puretek Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 15, 2025
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- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
- Directions
- Other information
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Inactive ingredients:
Aloe Barbadensis (Aloe Vera) Leaf Juice, Aqua (Purified Water), Borago Officinalis (Borage) Seed Oil, Carbomer, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, DL-Alpha Tocopheryl Acetate, Eucalyptus Globus Leaf Oil, Fructose, Phenoxyethanol, Propylene Glycol, Sodium Hydroxide, Squalane, Stearic Acid, Stearyl Alcohol, Tetrasodium EDTA, Vitis Vinifera (Grape) Seed Oil, Fragrance.
- Methyl Salicylate 25%
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INGREDIENTS AND APPEARANCE
METHYL SALICYLATE 25% PAIN RELIEVING
methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 250 mg in 1 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) STEARIC ACID (UNII: 4ELV7Z65AP) CETEARETH-20 (UNII: YRC528SWUY) AQUA (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) FRUCTOSE (UNII: 6YSS42VSEV) CETEARYL ALCOHOL (UNII: 2DMT128M1S) VITIS VINIFERA (GRAPE) SEED OIL (UNII: 930MLC8XGG) CARBOMER (UNII: 0A5MM307FC) CETYL ALCOHOL (UNII: 936JST6JCN) TETRASODIUM EDTA (UNII: MP1J8420LU) EUCALYPTUS GLOBULUS LEAF OIL (UNII: 2R04ONI662) ALOE VERA LEAF (UNII: ZY81Z83H0X) SQUALANE (UNII: GW89575KF9) BORAGO OFFICINALIS SEED OIL (UNII: F8XAG1755S) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-014-06 60 g in 1 JAR; Type 0: Not a Combination Product 06/12/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 06/12/2025 Labeler - Puretek Corporation (785961046)

