Hurricaine Liquid
NDC Package 0283-0569-72
Package Information
Hurricaine (benzocaine) liquids is do not exceed recommended dosageadults and children 2 years of age and older: apply to the affected area. Gargle, swish around in the mouth, or allow to remain in place at least 1 minute and then spit out. Use up to 4 times daily or as directed by a dentist or doctor children under 12 years of age: should be supervised in the use of the product children under 2 years of age: consult a dentist or doctor. This formulation utilizes a liquid delivery system. Marketed by Beutlich Pharmaceuticals, Llc, this product is identified by NDC 0283-0569 and is authorized under FDA application M022.
Identification & Billing
- RxCUI: 308657 - benzocaine 20 % Mucous Membrane Topical Solution
- RxCUI: 308657 - benzocaine 200 MG/ML Mucous Membrane Topical Solution
- RxCUI: 808062 - HurriCaine Oral Anesthetic 20 % Mucous Membrane Topical Solution
- RxCUI: 808062 - benzocaine 200 MG/ML Mucous Membrane Topical Solution [Hurricaine]
- RxCUI: 808062 - Hurricaine 20 % Mucous Membrane Topical Solution
Clinical Specifications
- Dental - Administration to a tooth or teeth.
- Oral - Administration to or by way of the mouth.
- Periodontal - Administration around a tooth.
Regulatory & Marketing
Hierarchy Structure
- 0283 - Beutlich Pharmaceuticals, Llc
- 0283-0569 - Hurricaine
- 0283-0569-72 - 72 g in 1 APPLICATOR
- 0283-0569 - Hurricaine
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 (0283-0569). 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 0283-0569-72 identifies a specific commercial package of 72 g in 1 applicator of Hurricaine Topical Anesthetic Liquid, a human over the counter drug labeled by Beutlich Pharmaceuticals, Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. This liquid is formulated for dental; oral; periodontal use and contains benzocaine 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 Beutlich Pharmaceuticals, Llc on May 15, 1969. The current certification is valid through December 31, 2026.
How is this Beutlich Pharmaceuticals, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00283056972. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. 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 Labeler segment to maintain the 5-4-2 structure.
