Label: PASMOL PAIN RELIEVING- menthol and methyl salicylate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 61361-820-03 - Packager: Grafor, Inc.
- 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 April 8, 2015
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- Active ingredients
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- Pasmol Pain Relieving Ointment, 85g (61361-820-03)
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INGREDIENTS AND APPEARANCE
PASMOL PAIN RELIEVING
menthol and methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61361-820 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 14 g in 100 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61361-820-03 85 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part348 04/08/2015 Labeler - Grafor, Inc. (135138811) Establishment Name Address ID/FEI Business Operations Grafor, Inc. 135138811 manufacture(61361-820)