NDC 41520-317

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 Car One. The primary component is Camphor (synthetic); Menthol; Methyl Salicylate.

Product ID41520-317_3690e974-3e64-4da6-9dc8-08fb23fa65b3
NDC41520-317
Product TypeHuman Otc Drug
Proprietary NameUltra Strength Pain Relief
Generic NameCamphor 4%, Menthol 10%, Methyl Salicylate 30%
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2014-08-26
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameCar One
Substance NameCAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Active Ingredient Strength4 g/100mL; g/100mL; g/100mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 41520-317-00

118 mL in 1 CAN (41520-317-00)
Marketing Start Date2014-08-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 41520-317-00 [41520031700]

Ultra Strength Pain Relief SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-08-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CAMPHOR (SYNTHETIC)4 g/100mL

OpenFDA Data

SPL SET ID:9509c8ee-bb4b-4b81-b21c-1671ce48f135
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1600127

    • 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%
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