Label: RINGMASTER RUBBING OIL- methyl salicylate liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 54947-124-31, 54947-124-32, 54947-124-33, 54947-124-34 - Packager: Painexx Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 February 22, 2018
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
- Directions
- Inactive ingredient
- Indications and usage
- Keep out reach of children
- Purpose
- Active ingredient
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RINGMASTER RUBBING OIL
methyl salicylate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54947-124 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 40 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:54947-124-31 30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/06/1950 2 NDC:54947-124-32 60 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/06/1950 3 NDC:54947-124-33 120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/06/1950 4 NDC:54947-124-34 240 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/06/1950 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 02/06/1950 Labeler - Painexx Corporation (080069233) Establishment Name Address ID/FEI Business Operations Painexx Corporation 080069233 manufacture(54947-124)
