NDC 73096-030

Flexible Pain Relief Roll-on Extra Strength

Pain Relief Roll-on Extra Strength

Flexible Pain Relief Roll-on Extra Strength is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Harmony Product Llc. The primary component is Menthol.

• Product ID: 73096-030_8c3d270f-4dfa-12fb-e053-2a95a90a7a7a
• NDC: 73096-030
• Product Type: Human Otc Drug
• Proprietary Name: Flexible Pain Relief Roll-on Extra Strength
• Generic Name: Pain Relief Roll-on Extra Strength
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-07-10
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Harmony Product LLC
• Substance Name: MENTHOL
• Active Ingredient Strength: 2126 mg/85.05g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 73096-030-02

1 BOTTLE, WITH APPLICATOR in 1 CARTON (73096-030-02) > 85.05 g in 1 BOTTLE, WITH APPLICATOR (73096-030-01)

• Marketing Start Date: 2019-07-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 73096-030-02 [73096003002]

Flexible Pain Relief Roll-on Extra Strength GEL

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-10

NDC 73096-030-01 [73096003001]

Flexible Pain Relief Roll-on Extra Strength GEL

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-10

Drug Details

Active Ingredients

Ingredient	Strength
MENTHOL	2126 mg/85.05g

OpenFDA Data

• SPL SET ID: 8c3d270f-4df9-12fb-e053-2a95a90a7a7a
• Manufacturer:
  • Harmony Product LLC
• UNII:
  • L7T10EIP3A
• UPC Code:
  • 0850003558516
  • 0850003558622
  • 0850003558493
  • 0850003558509
  • 0850003558646