NDC 58232-4024

Bengay Ultra Strength Non Greasy Pain Relieving

Camphor (synthetic), Menthol, And Methyl Salicylate

Bengay Ultra Strength Non Greasy Pain Relieving is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is Camphor (synthetic); Menthol, Unspecified Form; Methyl Salicylate.

Product ID58232-4024_20f17e01-7552-4662-af6c-ee69ddf9cd36
NDC58232-4024
Product TypeHuman Otc Drug
Proprietary NameBengay Ultra Strength Non Greasy Pain Relieving
Generic NameCamphor (synthetic), Menthol, And Methyl Salicylate
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2008-06-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameJohnson & Johnson Consumer Inc.
Substance NameCAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active Ingredient Strength40 mg/g; mg/g; mg/g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58232-4024-3

1 TUBE in 1 CARTON (58232-4024-3) > 57 g in 1 TUBE
Marketing Start Date2008-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58232-4024-1 [58232402401]

Bengay Ultra Strength Non Greasy Pain Relieving CREAM
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-06-01
Marketing End Date2019-11-02

NDC 58232-4024-5 [58232402405]

Bengay Ultra Strength Non Greasy Pain Relieving CREAM
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-08-07
Marketing End Date2015-09-01

NDC 58232-4024-2 [58232402402]

Bengay Ultra Strength Non Greasy Pain Relieving CREAM
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-06-01
Marketing End Date2010-08-08

NDC 58232-4024-3 [58232402403]

Bengay Ultra Strength Non Greasy Pain Relieving CREAM
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-06-01
Marketing End Date2020-02-23

Drug Details

Active Ingredients

IngredientStrength
CAMPHOR (SYNTHETIC)40 mg/g

OpenFDA Data

SPL SET ID:5aa265f8-ab45-47b2-b5ab-d4df54daed01
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 701976
  • 283083

    • NDC Crossover Matching brand name "Bengay Ultra Strength Non Greasy Pain Relieving" or generic name "Camphor (synthetic), Menthol, And Methyl Salicylate"

    NDCBrand NameGeneric Name
    58232-4024Bengay Ultra Strength Non Greasy Pain RelievingCamphor (Synthetic), Menthol, and Methyl Salicylate
    15478-111Apeaz Ultracamphor (synthetic), menthol, and methyl salicylate
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