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 ID: 58133-100_624ae049-7879-3713-e053-2991aa0a07bf
• NDC: 58133-100
• Product Type: Human Otc Drug
• Proprietary Name: Real Time Pain Relief MAXX Topical Analgesic
• Generic Name: Menthol 1.5%
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-01-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: Cosmetic Specialty Labs, Inc.
• Substance Name: MENTHOL
• Active Ingredient Strength: 2 g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 58133-100-04

120 mL in 1 TUBE (58133-100-04)

• Marketing Start Date: 2014-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58133-100-62 [58133010062]

Real Time Pain Relief MAXX Topical Analgesic LOTION

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-02-10

NDC 58133-100-16 [58133010016]

Real Time Pain Relief MAXX Topical Analgesic LOTION

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-01

NDC 58133-100-15 [58133010015]

Real Time Pain Relief MAXX Topical Analgesic LOTION

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-01

NDC 58133-100-60 [58133010060]

Real Time Pain Relief MAXX Topical Analgesic LOTION

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-02-10

NDC 58133-100-04 [58133010004]

Real Time Pain Relief MAXX Topical Analgesic LOTION

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-01

NDC 58133-100-12 [58133010012]

Real Time Pain Relief MAXX Topical Analgesic LOTION

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-01

NDC 58133-100-33 [58133010033]

Real Time Pain Relief MAXX Topical Analgesic LOTION

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-01-01

Drug Details

Active Ingredients

Ingredient	Strength
MENTHOL	1.5 g/100mL

OpenFDA Data

• SPL SET ID: 6180d7e4-1bc5-ffc5-e053-2991aa0af1b9
• Manufacturer:
  • Cosmetic Specialty Labs, Inc.
• UNII:
  • L7T10EIP3A
• 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%"

NDC	Brand Name	Generic Name
69711-008	MOBILITY	Menthol 1.5%
73672-989	Pain Relief Gel	Menthol 1.5%
58133-900	Real Time Pain Relief Foot Cream	Menthol 1.5%
58133-100	Real Time Pain Relief MAXX	Menthol 1.5%