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  4. NDC Product Code: 68093-7038 Stingeze Insect Bite Relief

NDC 68093-7038 Stingeze Insect Bite Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68093-7038?
  4. Stingeze Insect Bite Relief Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68093-7038
Proprietary Name:
Stingeze Insect Bite Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wisconsin Pharmacal Company
Labeler Code:
68093
Product Label ID:
dd633ca5-d7fb-4098-a0cc-26dfef6e7823
Start Marketing Date: [9]
02-01-2009
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 68093-7038?

The NDC code 68093-7038 is assigned by the FDA to the product Stingeze Insect Bite Relief which is product labeled by Wisconsin Pharmacal Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68093-7038-1 1 bottle, with applicator in 1 carton / 14.79 g in 1 bottle, with applicator. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Stingeze Insect Bite Relief?

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

Which are Stingeze Insect Bite Relief UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Stingeze Insect Bite Relief Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Stingeze Insect Bite Relief?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1435257 - benzocaine 5 % / camphor 3 % / phenol 1.35 % Topical Solution
  • RxCUI: 1435257 - benzocaine 50 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution
  • RxCUI: 1435262 - StingEze 5 % / 3 % / 1.35 % Topical Solution
  • RxCUI: 1435262 - benzocaine 50 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution [StingEze w/ Camphor]
  • RxCUI: 1435262 - StingEze w/ Camphor (benzocaine 5 % / camphor 3 % / phenol 1.35 % ) Topical Solution

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".