Label: TOPICAL ANALGESIC- methyl salicylate ointment
- NDC Code(s): 82165-100-02
- Packager: Dermaline USA Corp
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 3, 2023
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY
- Directions
- Other information
- Inactive ingredients
- STOP USE
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
TOPICAL ANALGESIC
methyl salicylate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82165-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 15 mg in 100 g Inactive Ingredients Ingredient Name Strength PROPYLPARABEN (UNII: Z8IX2SC1OH) WHITE PETROLATUM (UNII: B6E5W8RQJ4) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) WATER (UNII: 059QF0KO0R) ARNICA MONTANA (UNII: O80TY208ZW) EUCALYPTUS OIL (UNII: 2R04ONI662) MENTHOL (UNII: L7T10EIP3A) MINERAL OIL (UNII: T5L8T28FGP) PARAFFIN (UNII: I9O0E3H2ZE) TEA TREE OIL (UNII: VIF565UC2G) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82165-100-02 70 g in 1 JAR; Type 0: Not a Combination Product 05/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/15/2021 Labeler - Dermaline USA Corp (016069241)