Hurricaine Liquid
NDC Package 0283-1886-31
Package Information
Hurricaine (benzocaine) liquids is directionsdo not exceed recommended dosageadults and children 2 years of age and older: apply to the affected area. This formulation utilizes a liquid delivery system. Marketed by Beutlich Pharmaceuticals, Llc, this product is identified by NDC 0283-1886 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
- 0283-1886 - Hurricaine
- 0283-1886-31 - 29.6 g in 1 BOTTLE, PLASTIC
- 0283-1886 - 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.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0283-1886-31 identifies a specific commercial package of 29.6 g in 1 bottle, plastic of Hurricaine Topical Anesthetic Liquid, a human over the counter drug labeled by Beutlich Pharmaceuticals, Llc. 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 August 15, 1986. 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: 00283188631. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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.