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  4. NDC Product Code: 11822-3420 Renewal Daily Moisturizer Sensitive Skin

NDC 11822-3420 Renewal Daily Moisturizer Sensitive Skin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11822-3420?
  4. Renewal Daily Moisturizer Sensitive Skin Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11822-3420
Proprietary Name:
Renewal Daily Moisturizer Sensitive Skin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid Corporation
Labeler Code:
11822
Product Label ID:
6a0d70fc-e70e-4c53-a9a9-82c5be533e33
Start Marketing Date: [9]
07-21-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11822-3420-2

Package Description: 50 mL in 1 BOTTLE

Product Details

What is NDC 11822-3420?

The NDC code 11822-3420 is assigned by the FDA to the product Renewal Daily Moisturizer Sensitive Skin which is product labeled by Rite Aid Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-3420-2 50 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 Renewal Daily Moisturizer Sensitive Skin?

APPLY LIBERALLY ON FACE, NECK AND OTHER EXPOSED AREAS EVERY MORNING AFTER CLEANSING.  REAPPLY IF EXCESS PERSPIRATION OR PRODUCT WEARS OCCURS.  PERFECT ALONE OR UNDER MAKEUP OR OVER A SERUM.  FOR SUNSCREEN BENEFITS, APPLY PRIOR TO SUN EXPOSURE.

Which are Renewal Daily Moisturizer Sensitive Skin UNII Codes?

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

Which are Renewal Daily Moisturizer Sensitive Skin 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:

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Patient Education

Guaifenesin


Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
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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".