NDC 64048-5114

Ultra Strength Pain Relief

Camphor 4%, Menthol 10%, Methyl Salicylate 30%

Ultra Strength Pain Relief is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Product Quest Mfg. The primary component is Camphor (synthetic); Menthol; Methyl Salicylate.

Product ID64048-5114_2c4c25cc-4283-435e-a614-1cad8d1338f6
NDC64048-5114
Product TypeHuman Otc Drug
Proprietary NameUltra Strength Pain Relief
Generic NameCamphor 4%, Menthol 10%, Methyl Salicylate 30%
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2014-02-06
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameProduct Quest Mfg
Substance NameCAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Active Ingredient Strength4 g/100g; g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 64048-5114-4

113 g in 1 CAN (64048-5114-4)
Marketing Start Date2014-02-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64048-5114-4 [64048511404]

Ultra Strength Pain Relief SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-02-06
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CAMPHOR (SYNTHETIC)4 g/100g

OpenFDA Data

SPL SET ID:4a595401-20af-437e-a658-44e9358d9008
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1600127
  • UPC Code
  • 0727510004426
  • NDC Crossover Matching brand name "Ultra Strength Pain Relief" or generic name "Camphor 4%, Menthol 10%, Methyl Salicylate 30%"

    NDCBrand NameGeneric Name
    41520-317Ultra Strength Pain ReliefCamphor 4%, Menthol 10%, Methyl Salicylate 30%
    52000-135ULTRA STRENGTH PAIN RELIEFcapsaicin
    64048-5114Ultra Strength Pain ReliefCamphor 4%, Menthol 10%, Methyl Salicylate 30%
    71183-135ULTRA STRENGTH PAIN RELIEFcapsaicin
    72839-147Warrior Pain RelievingCamphor 4%, Menthol 10%, Methyl Salicylate 30%

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.