NDC 51068-501

ActivOn Ultra Strength Arthritis

Menthol And Histamine Dihydrochloride

ActivOn Ultra Strength Arthritis is a Topical Stick in the Human Otc Drug category. It is labeled and distributed by Family First Pharmaceuticals, Inc.. The primary component is Menthol, Unspecified Form; Histamine Dihydrochloride.

• Product ID: 51068-501_6a97a677-5c25-4d3a-9593-3191f6a981bd
• NDC: 51068-501
• Product Type: Human Otc Drug
• Proprietary Name: ActivOn Ultra Strength Arthritis
• Generic Name: Menthol And Histamine Dihydrochloride
• Dosage Form: Stick
• Route of Administration: TOPICAL
• Marketing Start Date: 2011-09-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: Family First Pharmaceuticals, Inc.
• Substance Name: MENTHOL, UNSPECIFIED FORM; HISTAMINE DIHYDROCHLORIDE
• Active Ingredient Strength: 0 g/g; g/g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51068-501-01

1 CANISTER in 1 CARTON (51068-501-01) > 57 g in 1 CANISTER

• Marketing Start Date: 2011-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51068-501-01 [51068050101]

ActivOn Ultra Strength Arthritis STICK

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-09-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	.04574 g/g

OpenFDA Data

• SPL SET ID: d123deae-d9ef-45ce-81ed-2d79384b1298
• Manufacturer:
  • Family First Pharmaceuticals, Inc.
• UNII:
  • 3POA0Q644U
  • L7T10EIP3A
• RxNorm Concept Unique ID - RxCUI:
  • 1148636
  • 1148634
• UPC Code:
  • 0854822025013

NDC Crossover Matching brand name "ActivOn Ultra Strength Arthritis" or generic name "Menthol And Histamine Dihydrochloride"

NDC	Brand Name	Generic Name
51068-501	ActivOn Ultra Strength Arthritis	Menthol and Histamine Dihydrochloride
51068-507	ActivOn Ultra Strength Arthritis	Menthol, Unspecified Form