Label: METHYL SALICYLATE 25% CREAM- methyl salicylate 25% cream
- NDC Code(s): 81877-721-01
- Packager: Forreal Pharmaceuticals LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 2, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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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
- Directions
- Other information
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Inactive ingredients
Aloe vera leaf, Glycerine, Arnica Montana Flower, Indian Frankincense, Cetostearyl Alcohol, Ethylhexylglycerin, Glucosamine Sulfate, Glyceryl Monostearate, C13-14 Isoparaffin, Isosteryl Palmitate, Trolamine, Stearic Acid, Propylene Glycol, Laureth-7, Peg-100 Stearate, Water, Phenoxyethanol
Methyl Salicylate 25% Cream
NDC: 81877-721-01
120 grams
Manufactured for:
Forreal Pharmaceuticals, LLC
Royal Oak, MI 48067 - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
METHYL SALICYLATE 25% CREAM
methyl salicylate 25% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81877-721 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) ISOSTEARYL PALMITATE (UNII: 9EHU0R7ER1) TROLAMINE (UNII: 9O3K93S3TK) STEARIC ACID (UNII: 4ELV7Z65AP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) LAURETH-7 (UNII: Z95S6G8201) PEG-100 STEARATE (UNII: YD01N1999R) WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81877-721-01 120 g in 1 BOTTLE; Type 0: Not a Combination Product 04/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug part348 04/15/2024 Labeler - Forreal Pharmaceuticals LLC (118029197)