NDC 71262-004

Liberdol Analgesic

Menthol, Unspecified Form, Methyl Salicylate

Liberdol Analgesic is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Viaderma Distribution, Inc.. The primary component is Camphor (synthetic); Menthol, Unspecified Form; Methyl Salicylate.

Product ID71262-004_94199fb0-8911-d3cd-e053-2a95a90aeb90
NDC71262-004
Product TypeHuman Otc Drug
Proprietary NameLiberdol Analgesic
Generic NameMenthol, Unspecified Form, Methyl Salicylate
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2019-10-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameViaDerma Distribution, Inc.
Substance NameCAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active Ingredient Strength40 mg/mL; mg/mL; mg/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71262-004-18

118 mL in 1 BOTTLE, SPRAY (71262-004-18)
Marketing Start Date2019-10-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71262-004-18 [71262000418]

Liberdol Analgesic LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-01

Drug Details

Active Ingredients

IngredientStrength
CAMPHOR (SYNTHETIC)40 mg/mL

OpenFDA Data

SPL SET ID:69b35410-577f-4553-bd85-49ef31555aeb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1600127
  • UPC Code
  • 0865393000408

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