1. Home
  2. Labeler Index
  3. Insight Pharmaceuticals
  4. NDC Product Code: 63736-293 Skin Shield

NDC 63736-293 Skin Shield

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63736-293?
  5. Skin Shield Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
63736-293
Proprietary Name:
Skin Shield
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Insight Pharmaceuticals
Labeler Code:
63736
Product Label ID:
bc596cfe-1229-42c1-940b-c40a81ead64f
Start Marketing Date: [9]
06-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 63736-293-24

Package Description: 24 BOX in 1 CASE / 1 BOTTLE in 1 BOX / 26.9 mL in 1 BOTTLE

NDC Code 63736-293-36

Package Description: 36 BOX in 1 CASE / 1 BOTTLE in 1 BOX / 29.6 mL in 1 BOTTLE

Product Details

What is NDC 63736-293?

The NDC code 63736-293 is assigned by the FDA to the product Skin Shield which is product labeled by Insight Pharmaceuticals. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 63736-293-24 24 box in 1 case / 1 bottle in 1 box / 26.9 ml in 1 bottle, 63736-293-36 36 box in 1 case / 1 bottle in 1 box / 29.6 ml in 1 bottle. 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 Skin Shield?

Adults and children 2 years of age and older:Clean the affected area.Dry thoroughly.Brush a small amount of product on the area 1 to 3 times daily and let dry.Hold knees, elbows, knuckles in bent position during application and drying.For more protection, apply second coat.Children under 2 years of age:Consult a doctor.

Which are Skin Shield UNII Codes?

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

Which are Skin Shield 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 Skin Shield?

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: 1048366 - benzethonium Cl 0.2 % / dyclonine HCl 0.75 % Topical Solution
  • RxCUI: 1048366 - benzethonium chloride 2 MG/ML / dyclonine hydrochloride 7.5 MG/ML Topical Solution
  • RxCUI: 1053196 - Skin Shield 0.2 % / 0.75 % Topical Solution
  • RxCUI: 1053196 - benzethonium chloride 2 MG/ML / dyclonine hydrochloride 7.5 MG/ML Topical Solution [Skin Shield]
  • RxCUI: 1053196 - Skin Shield (benzethonium Cl 0.2 % / dyclonine HCl 0.75 % ) Liquid Bandage

* 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".