Curist 5% Lidocaine Spray
NDC Package 72559-034-57
Package Information
Curist 5% Lidocaine (lidocaine 5%) sprays is usestemporarily shrinks hemorrhoidal tissue ■ temporarily reduces the swelling associated with irritation in hemorrhoids and other anorectal disorders ■ for the temporary relief of pain ■ for the temporary relief of local itching and discomfort in the perianal area. This formulation utilizes a spray delivery system. Marketed by Little Pharma, Inc., this product is identified by NDC 72559-034 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 2168528 - lidocaine HCl 5 % / phenylephrine HCl 0.25 % Topical Spray
- RxCUI: 2168528 - lidocaine hydrochloride 50 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Topical Spray
- RxCUI: 2168528 - lidocaine hydrochloride 5 % / phenylephrine hydrochloride 0.25 % Topical Spray
Clinical Specifications
- Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
- Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
- Amides - [CS]
- Antiarrhythmic - [EPC] (Established Pharmacologic Class)
- Local Anesthesia - [PE] (Physiologic Effect)
- alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 72559 - Little Pharma, Inc.
- 72559-034 - Curist 5% Lidocaine
- 72559-034-57 - 177 mL in 1 CAN
- 72559-034 - Curist 5% Lidocaine
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 72559-034-57 identifies a specific commercial package of 177 ml in 1 can of Curist 5% Lidocaine, a human over the counter drug labeled by Little Pharma, Inc.. This spray is formulated for topical use and contains lidocaine hydrochloride; phenylephrine hydrochloride 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 Little Pharma, Inc. on December 27, 2023. The current certification is valid through December 31, 2026.
How is this Little Pharma, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 72559003457. 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.