Label: METHYL SALICYLATE cream
- NDC Code(s): 50488-1015-1, 50488-1015-5
- Packager: Alexso, Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 1, 2022
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only.
When using this product
- Avoid contact with the eyes
- Do not use in large quantities, particularly over raw surfaces or blistered areas
- Do not apply to wounds or damaged skin
- Do not bandage
- Avoid contact with the eyes
- Directions
- Other information
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Inactive ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cetearyl Alcohol, Chondroitin Sulfate, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, C13-14 Isoparaffin, Isostearyl Palmitate, Laureth-7, Methylsulfonylmethane (MSM), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Sodium Polyacrylate, Stearic Acid, Triethanolamine
Methyl Salicylate 25% Cream
NDC: 50488-1015-5
50 grams
Methyl Salicylate 25% Cream
NDC: 50488-1015-1
120 grams
Manufactured for:
Alexso, Inc
Los Angeles, CA 90064 - PRINCIPAL DISPLAY PANEL
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
METHYL SALICYLATE
methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50488-1015 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 WATER (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) ISOSTEARYL PALMITATE (UNII: 9EHU0R7ER1) LAURETH-7 (UNII: Z95S6G8201) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STEARIC ACID (UNII: 4ELV7Z65AP) TROLAMINE (UNII: 9O3K93S3TK) CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50488-1015-1 120 g in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2019 2 NDC:50488-1015-5 50 g in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/01/2019 Labeler - Alexso, Inc (963338061)