1. Home
  2. Labeler Index
  3. Crawford Healthcare, Inc.
  4. NDC Product Code: 69502-004 Touchless Care Zinc Oxide Protectant

NDC 69502-004 Touchless Care Zinc Oxide Protectant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69502-004?
  4. Touchless Care Zinc Oxide Protectant 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:
69502-004
Proprietary Name:
Touchless Care Zinc Oxide Protectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Crawford Healthcare, Inc.
Labeler Code:
69502
Product Label ID:
215c8b9f-9c0a-053a-e054-00144ff8d46c
Start Marketing Date: [9]
12-04-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69502-004-28

Package Description: 128 g in 1 BOTTLE, SPRAY

NDC Code 69502-004-57

Package Description: 57 g in 1 BOTTLE, SPRAY

Product Details

What is NDC 69502-004?

The NDC code 69502-004 is assigned by the FDA to the product Touchless Care Zinc Oxide Protectant which is product labeled by Crawford Healthcare, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69502-004-28 128 g in 1 bottle, spray , 69502-004-57 57 g in 1 bottle, spray . 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 Touchless Care Zinc Oxide Protectant?

Cleanse skin area and allow to dry.Shake bottle well before use.Spray 4-6 inches from skin. No rub-in is required.Apply liberally as often as necessary.

Which are Touchless Care Zinc Oxide Protectant UNII Codes?

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

Which are Touchless Care Zinc Oxide Protectant 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 Touchless Care Zinc Oxide Protectant?

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: 968817 - dimethicone 20 % / zinc oxide 25 % Topical Spray
  • RxCUI: 968817 - dimethicone 200 MG/ML / zinc oxide 250 MG/ML Topical Spray
  • RxCUI: 968817 - dimethicone 200 MG/ML / ZNO 250 MG/ML Topical Spray

* 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".