NDC 11822-8011 Body Wash Clear Spring

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11822-8011
Proprietary Name:
Body Wash Clear Spring
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid Corporation
Labeler Code:
11822
Start Marketing Date: [9]
09-22-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)

Product Packages

NDC Code 11822-8011-2

Package Description: 355 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 11822-8011?

The NDC code 11822-8011 is assigned by the FDA to the product Body Wash Clear Spring 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 11822-8011-2 355 ml in 1 bottle, plastic . 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 Body Wash Clear Spring?

- squeeze onto wet hands or body sponge- work into a lather- wash skin, rinse, and dry thoroughly

Which are Body Wash Clear Spring UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Body Wash Clear Spring?

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".