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  4. NDC Product Code: 55118-703 Scott Moisturizing Foam Hand Sanitizer

NDC 55118-703 Scott Moisturizing Foam Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55118-703?
  4. Scott Moisturizing Foam Hand Sanitizer 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:
55118-703
Proprietary Name:
Scott Moisturizing Foam Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kimberly-clark Corporation
Labeler Code:
55118
Product Label ID:
d481c4bb-78a8-4941-a712-18881f7f0610
Start Marketing Date: [9]
09-01-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 55118-703-12

Package Description: 1200 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 55118-703?

The NDC code 55118-703 is assigned by the FDA to the product Scott Moisturizing Foam Hand Sanitizer which is product labeled by Kimberly-clark Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55118-703-12 1200 ml in 1 bottle, pump . 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 Scott Moisturizing Foam Hand Sanitizer?

Use enough foam to cover your hands. Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. Use as part of your daily cleansing routine.

Which are Scott Moisturizing Foam Hand Sanitizer UNII Codes?

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

Which are Scott Moisturizing Foam Hand Sanitizer 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 Scott Moisturizing Foam Hand Sanitizer?

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:

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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".