Stingeze
NDC Package 68093-7151-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Stingeze is clean areaApply a small amount to the bite area while massaging with sponge tip applicator.  If itching persists, apply again in 10-15 minutesFor ticks and bees, remove tick or stinger before treatmentAdults and children 2 years and over: Apply to affected area 1 to 3 times dailyChildren under 2 years: Consult a doctor. Marketed by Wisconsin Pharmacal Company, this product is identified by NDC 68093-7151 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
68093-7151-1
Package Description
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 14.8 g in 1 BOTTLE, WITH APPLICATOR
Product Code
68093-7151
11-Digit Billing Format
68093715101
RxNorm Crosswalk
  • RxCUI: 1485210 - benzocaine 10 % / camphor 3 % / phenol 1.35 % Topical Solution
  • RxCUI: 1485210 - benzocaine 100 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution
  • RxCUI: 1485215 - StingEze MAX 10 % / 3 % / 1.35 % Topical Solution
  • RxCUI: 1485215 - benzocaine 100 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution [Stingeze Max]
  • RxCUI: 1485215 - Stingeze Max (benzocaine 10 % / camphor 3 % / phenol 1.35 % ) Topical Solution

Clinical Specifications

Proprietary Name
Stingeze Max Insect Bite Relief
Dosage Form
-
Usage Information
Clean areaApply a small amount to the bite area while massaging with sponge tip applicator.  If itching persists, apply again in 10-15 minutesFor ticks and bees, remove tick or stinger before treatmentAdults and children 2 years and over: Apply to affected area 1 to 3 times dailyChildren under 2 years: Consult a doctor

Regulatory & Marketing

Labeler Name
Wisconsin Pharmacal Company
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
02-01-2009
Listing Expiration
12-31-2019
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 68093-7151-1 identifies a specific commercial package of 1 bottle, with applicator in 1 carton / 14.8 g in 1 bottle, with applicator of Stingeze Max Insect Bite Relief, labeled by Wisconsin Pharmacal Company. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Wisconsin Pharmacal Company on February 01, 2009. The current certification is valid through December 31, 2019.

How is this Wisconsin Pharmacal Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68093715101. 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:

10-Digit Format (5-4-1)
68093-7151-1
11-Digit CMS (5-4-2)
68093-7151-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.