Ora Yogu 4x Medicated Tooth And Gum Pain Reliever Gel
NDC Package 87351-761-10
Package Information
Ora Yogu 4x Medicated Tooth And Gum Pain Reliever (medicated tooth and gum pain reliever) gel is adult and children 2 years of age and over - Apply to affected area up to 4 times daily or as directed by a dentist or doctor.Children between 2 and 12 years of age - Ask a doctor before use. This formulation utilizes a gel delivery system. Marketed by Kungpo Health Care & Herbal Center Inc, this product is identified by NDC 87351-761 and is authorized under FDA application M022.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 87351 - Kungpo Health Care & Herbal Center Inc
- 87351-761 - Ora Yogu 4x Medicated Tooth And Gum Pain Reliever
- 87351-761-10 - 1 TUBE in 1 PACKAGE / 10 mL in 1 TUBE
- 87351-761 - Ora Yogu 4x Medicated Tooth And Gum Pain Reliever
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 87351-761-10 identifies a specific commercial package of 1 tube in 1 package / 10 ml in 1 tube of Ora Yogu 4x Medicated Tooth And Gum Pain Reliever, a human over the counter drug labeled by Kungpo Health Care & Herbal Center Inc. This gel is formulated for topical use and contains benzalkonium chloride; benzocaine; menthol; zinc chloride 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 Kungpo Health Care & Herbal Center Inc on April 15, 2026. The current certification is valid through December 31, 2027.
How is this Kungpo Health Care & Herbal Center Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 87351076110. 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.