NDC 69968-0539

Listerine Ultraclean Antiseptic Cool Mint

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

Listerine Ultraclean Antiseptic Cool 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: 69968-0539_5019e485-ffac-4558-a462-434f73637384
• NDC: 69968-0539
• Product Type: Human Otc Drug
• Proprietary Name: Listerine Ultraclean Antiseptic Cool Mint
• Generic Name: Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, And Thymol
• Dosage Form: Mouthwash
• Route of Administration: ORAL
• Marketing Start Date: 2012-06-01
• 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 69968-0539-1

1000 mL in 1 BOTTLE, PLASTIC (69968-0539-1)

• Marketing Start Date: 2012-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69968-0539-5 [69968053905]

Listerine Ultraclean Antiseptic Cool Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-06-01

NDC 69968-0539-3 [69968053903]

Listerine Ultraclean Antiseptic Cool Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-06-01

NDC 69968-0539-1 [69968053901]

Listerine Ultraclean Antiseptic Cool Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-06-01

NDC 69968-0539-2 [69968053902]

Listerine Ultraclean Antiseptic Cool Mint MOUTHWASH

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-06-01

Drug Details

Active Ingredients

Ingredient	Strength
EUCALYPTOL	.92 mg/mL

OpenFDA Data

• SPL SET ID: dd3729c2-fd05-4db0-a542-487bb0f9001f
• Manufacturer:
  • Johnson & Johnson Consumer Inc.
• UNII:
  • L7T10EIP3A
  • 3J50XA376E
  • RV6J6604TK
  • LAV5U5022Y
• RxNorm Concept Unique ID - RxCUI:
  • 1043619
  • 2043303
• UPC Code:
  • 0312547422680

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

NDC	Brand Name	Generic Name
42002-447	Listerine Ultraclean Antiseptic Cool Mint	Listerine Ultraclean Antiseptic Cool Mint
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
69968-0399	Listerine Ultraclean Arctic Mint	Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol
69968-0398	Listerine Ultraclean Fresh Citrus	Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol