NDC 58133-956

RelieveIt Footspray Topical Analgesic

Menthol 8%

RelieveIt Footspray Topical Analgesic is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Cosmetic Specialty Labs, Inc.. The primary component is Menthol.

• Product ID: 58133-956_a0c0b3e2-d72e-81bf-e053-2995a90ad9a0
• NDC: 58133-956
• Product Type: Human Otc Drug
• Proprietary Name: RelieveIt Footspray Topical Analgesic
• Generic Name: Menthol 8%
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2020-03-13
• 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: 1 mg/15mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 58133-956-01

30 mL in 1 CARTON (58133-956-01)

• Marketing Start Date: 2020-03-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58133-956-02 [58133095602]

RelieveIt Footspray Topical Analgesic LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-03-13

NDC 58133-956-01 [58133095601]

RelieveIt Footspray Topical Analgesic LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
MENTHOL	1.2 mg/15mL

OpenFDA Data

• SPL SET ID: a0c0cbac-6adf-d85d-e053-2995a90a5da5
• Manufacturer:
  • Cosmetic Specialty labs, Inc.
• UNII:
  • L7T10EIP3A
• UPC Code:
  • 0861729000166
  • 0861729000104

NDC Crossover Matching brand name "RelieveIt Footspray Topical Analgesic" or generic name "Menthol 8%"

NDC	Brand Name	Generic Name
73287-014	Hempvana Ultra Strength Pain Relief Gel - Arthritis	Menthol 8%
58133-956	RelieveIt Footspray	Menthol 8%