Label: NAMMAN MUAY ATHLETES PAIN RELIEVING- menthol, methyl salicylate liniment
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Contains inactivated NDC Code(s)
NDC Code(s): 43599-001-04 - Packager: Devakam Apothecary Hall, Co, Ltd.
- 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 6, 2015
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- Official Label (Printer Friendly)
- NAMMAN MUAY Athlete's Pain Relieving Liniment
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only. Avoid contact with the eyes and mucous membranes
Ask a doctor before use if you have allergic reactions to aspirin or salicylates.
When using this product
- use only as directed
- do not bandage tightly or use with a heating pad
- do not apply to wounds or damaged skin
Stop use and ask a doctor if
- condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
- redness is present
- irritation of the skin develops
If pregnant or breast-feeding, ask a health professional before use.
- Directions
- Inactive Ingredients
- Namman Muay: 120ml
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INGREDIENTS AND APPEARANCE
NAMMAN MUAY ATHLETES PAIN RELIEVING
menthol, methyl salicylate linimentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43599-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 12.5 mg in 1 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 310 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) .BETA.-CAROTENE (UNII: 01YAE03M7J) EUCALYPTUS OIL (UNII: 2R04ONI662) MINERAL OIL (UNII: T5L8T28FGP) POLYSORBATE 80 (UNII: 6OZP39ZG8H) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43599-001-04 120 mL in 1 BOTTLE; 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 06/10/2011 Labeler - Devakam Apothecary Hall, Co, Ltd. (661733091) Registrant - Devakam Apothecary Hall, Co, Ltd. (661733091) Establishment Name Address ID/FEI Business Operations Devakam Apothecary Hall, Co, Ltd. 661733091 manufacture(43599-001)