Label: METHYL SALICYLATE 30% oil
- NDC Code(s): 81877-830-04
- Packager: FORREAL PHARMACEUTICALS LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 6, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions: Adults and children 12 years of age and older; apply generously to affected area. Massage vigorously into painful areas until absorbed completely. Repeat as needed, but do not use more than three times daily. Children under 12 years of age, ask a doctor.
Other information: Store at room temperature. Protect from light and heat. Close cap tightly after use.
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
METHYL SALICYLATE 30%
methyl salicylate 30% oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81877-830 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 30 g in 100 mL Inactive Ingredients Ingredient Name Strength PEANUT OIL (UNII: 5TL50QU0W4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81877-830-04 118 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/01/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2026 Labeler - FORREAL PHARMACEUTICALS LLC (118029197)

