Antiseptic Mouthrinse Mouthwash
NDC Package 69892-072-86
Package Information
Antiseptic Mouthrinse (eucalyptol, menthol, methyl salicylate, thymol) mouthwashes is adults and children under 12 years if age and older - vigorously swish 20 ml (2/3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds then spit out; do not swallowchildren under 12 years of age - consult a dentist or doctorthis rinse is not intended to replace brushing or flossing. This formulation utilizes a mouthwash delivery system. Marketed by Rockland Cosmetics, Inc., this product is identified by NDC 69892-072 and is authorized under FDA application 505G(a)(3).
Identification & Billing
- RxCUI: 1043619 - eucalyptol 0.092 % / menthol 0.042 % / methyl salicylate 0.06 % / thymol 0.064 % Mouthwash
- RxCUI: 1043619 - eucalyptol 0.92 MG/ML / menthol 0.42 MG/ML / methyl salicylate 0.6 MG/ML / thymol 0.64 MG/ML Mouthwash
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69892 - Rockland Cosmetics, Inc.
- 69892-072 - Antiseptic Mouthrinse
- 69892-072-86 - 1000 mL in 1 BOTTLE, PLASTIC
- 69892-072 - Antiseptic Mouthrinse
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (69892-072). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 69892-072-86 identifies a specific commercial package of 1000 ml in 1 bottle, plastic of Antiseptic Mouthrinse, a human over the counter drug labeled by Rockland Cosmetics, Inc.. This mouthwash is formulated for oral use and contains eucalyptol; menthol; methyl salicylate; thymol as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Rockland Cosmetics, Inc. on May 15, 2024. The current certification is valid through December 31, 2027.
How is this Rockland Cosmetics, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69892007286. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.