NDC 58133-100

Real Time Pain Relief MAXX Topical Analgesic

Menthol 1.5%

Real Time Pain Relief MAXX Topical Analgesic is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Cosmetic Specialty Labs, Inc.. The primary component is Menthol.

Product ID58133-100_624ae049-7879-3713-e053-2991aa0a07bf
NDC58133-100
Product TypeHuman Otc Drug
Proprietary NameReal Time Pain Relief MAXX Topical Analgesic
Generic NameMenthol 1.5%
Dosage FormLotion
Route of AdministrationTOPICAL
Marketing Start Date2014-01-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameCosmetic Specialty Labs, Inc.
Substance NameMENTHOL
Active Ingredient Strength2 g/100mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58133-100-04

120 mL in 1 TUBE (58133-100-04)
Marketing Start Date2014-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58133-100-62 [58133010062]

Real Time Pain Relief MAXX Topical Analgesic LOTION
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-10

NDC 58133-100-16 [58133010016]

Real Time Pain Relief MAXX Topical Analgesic LOTION
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-01

NDC 58133-100-15 [58133010015]

Real Time Pain Relief MAXX Topical Analgesic LOTION
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-01

NDC 58133-100-60 [58133010060]

Real Time Pain Relief MAXX Topical Analgesic LOTION
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-10

NDC 58133-100-04 [58133010004]

Real Time Pain Relief MAXX Topical Analgesic LOTION
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-01

NDC 58133-100-12 [58133010012]

Real Time Pain Relief MAXX Topical Analgesic LOTION
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-01

NDC 58133-100-33 [58133010033]

Real Time Pain Relief MAXX Topical Analgesic LOTION
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01

Drug Details

Active Ingredients

IngredientStrength
MENTHOL1.5 g/100mL

OpenFDA Data

SPL SET ID:6180d7e4-1bc5-ffc5-e053-2991aa0af1b9
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1148429
  • UPC Code
  • 0742832066303
  • NDC Crossover Matching brand name "Real Time Pain Relief MAXX Topical Analgesic" or generic name "Menthol 1.5%"

    NDCBrand NameGeneric Name
    69711-008MOBILITYMenthol 1.5%
    73672-989Pain Relief GelMenthol 1.5%
    58133-900Real Time Pain Relief Foot CreamMenthol 1.5%
    58133-100Real Time Pain Relief MAXXMenthol 1.5%

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