NDC 52316-028

Vortex

Toothpaste

Vortex is a Dental Paste, Dentifrice in the Human Otc Drug category. It is labeled and distributed by Dsc Laboratories, Div. Of Dsc Products Inc.. The primary component is Sodium Fluoride.

• Product ID: 52316-028_8ecf77c1-f102-4992-a08e-6f3d42a6036b
• NDC: 52316-028
• Product Type: Human Otc Drug
• Proprietary Name: Vortex
• Generic Name: Toothpaste
• Dosage Form: Paste, Dentifrice
• Route of Administration: DENTAL
• Marketing Start Date: 2011-12-30
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part355
• Labeler Name: DSC Laboratories, Div. of DSC Products Inc.
• Substance Name: SODIUM FLUORIDE
• Active Ingredient Strength: 2 mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 52316-028-42

120 g in 1 TUBE (52316-028-42)

• Marketing Start Date: 2011-12-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52316-028-42 [52316002842]

Vortex PASTE, DENTIFRICE

• Marketing Category: OTC monograph final
• Application Number: part355
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-30
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM FLUORIDE	2 mg/g

OpenFDA Data

• SPL SET ID: 47aef72b-2f09-4d08-b2d2-01b32e9e9faf
• Manufacturer:
  • DSC Laboratories, Div. of DSC Products Inc.
• UNII:
  • 8ZYQ1474W7
• RxNorm Concept Unique ID - RxCUI:
  • 1235783
• UPC Code:
  • 0742272001001

NDC Crossover Matching brand name "Vortex" or generic name "Toothpaste"

NDC	Brand Name	Generic Name
52316-028	Vortex	Toothpaste
71112-003	BEYOU Orange	Toothpaste
71112-002	BEYOU Pink	Toothpaste
65517-2000	Sodium fluoride	Toothpaste
53567-6044	SuperSmile Professional	Toothpaste