NDC 69968-0399

Listerine Ultraclean Arctic Mint

Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, And Thymol

Listerine Ultraclean Arctic Mint is a Oral Mouthwash in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is Eucalyptol; Menthol, Unspecified Form; Methyl Salicylate; Thymol.

• Product ID: 69968-0399_55c0af97-c480-499a-9ace-9c7248a1ee4b
• NDC: 69968-0399
• Product Type: Human Otc Drug
• Proprietary Name: Listerine Ultraclean Arctic Mint
• Generic Name: Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, And Thymol
• Dosage Form: Mouthwash
• Route of Administration: ORAL
• Marketing Start Date: 2012-07-03
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Johnson & Johnson Consumer Inc.
• Substance Name: EUCALYPTOL; MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE; THYMOL
• Active Ingredient Strength: 1 mg/mL; mg/mL; mg/mL; mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69968-0399-1

1000 mL in 1 BOTTLE, PLASTIC (69968-0399-1)

• Marketing Start Date: 2012-07-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69968-0399-1 [69968039901]

Listerine Ultraclean Arctic Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-03

NDC 69968-0399-9 [69968039909]

Listerine Ultraclean Arctic Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-03

NDC 69968-0399-2 [69968039902]

Listerine Ultraclean Arctic Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-03

NDC 69968-0399-3 [69968039903]

Listerine Ultraclean Arctic Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-03

NDC 69968-0399-8 [69968039908]

Listerine Ultraclean Arctic Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-03

Drug Details

Active Ingredients

Ingredient	Strength
EUCALYPTOL	.92 mg/mL

OpenFDA Data

• SPL SET ID: be6ea17b-2b72-4354-a2fa-e3aac0d5d7d9
• Manufacturer:
  • Johnson & Johnson Consumer Inc.
• UNII:
  • L7T10EIP3A
  • 3J50XA376E
  • RV6J6604TK
  • LAV5U5022Y
• RxNorm Concept Unique ID - RxCUI:
  • 1043619
  • 2043303
• UPC Code:
  • 0312547422598

NDC Crossover Matching brand name "Listerine Ultraclean Arctic Mint" or generic name "Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, And Thymol"

NDC	Brand Name	Generic Name
69968-0399	Listerine Ultraclean Arctic Mint	Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol
66715-6861	Antiseptic	Eucalyptol, Menthol, Unspecified Form, Methyl salicylate, and Thymol
69968-0400	LISTERINE	Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol
69968-0477	Listerine Cool Mint Antiseptic	Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol
69968-0550	Listerine Cool Mint Antiseptic	Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol
69968-0239	Listerine FreshBurst Antiseptic	Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol
69968-0604	Listerine Gum Therapy Antiseptic	eucalyptol, menthol, unspecified form, methyl salicylate, and thymol
69968-0605	Listerine Naturals Antiseptic	Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol
69968-0539	Listerine Ultraclean Antiseptic	Eucalyptol, Menthol, unspecified form, Methyl Salicylate, and Thymol
69968-0398	Listerine Ultraclean Fresh Citrus	Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol