Label: FRICCILICONT- menthol, methyl salicylate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 53038-001-10 - Packager: Labocont Industrial
- Category: HUMAN OTC DRUG LABEL
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 December 21, 2017
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor
- If pregnant or breast-feeding
- Keep out of reach of children.
- Directions
- Inactive Ingredients
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PRINCIPAL DISPLAY PANEL
SHAKE
DO NOT DRINKOintment
Friccilicont
EXTERNAL ANALGESIC
EFFECTIVE AND REINFORCEDLABOCONT
INDUSTRIAL
Sto. Dgo., Rep. Dom.LABORATORIOS, C. x A.
Made In Dominican Republic
Net Wt 10 oz (284 g)
MADE IN DOMINICAN REPUBLIC
MANUFACTURED FOR LABOCONT INDUSTRIAL, Km 19, Autopista las Americas, La Caleta. Sto. Dgo
DOMINICAN REPUBLIC TO REPORT A SERIOUS ADVERSE EVENT CONTACT 8109-756-7371 -
INGREDIENTS AND APPEARANCE
FRICCILICONT
menthol, methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53038-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 3 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP) TURPENTINE (UNII: XJ6RUH0O4G) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53038-001-10 284 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/15/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 08/15/2012 Labeler - Labocont Industrial (871485509)