1. Home
  2. Labeler Index
  3. Meijer Distribution, Inc
  4. NDC Product Code: 41250-642 Meijer Oatmeal Bath Skin Protectant

NDC 41250-642 Meijer Oatmeal Bath Skin Protectant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 41250-642?
  5. Meijer Oatmeal Bath Skin Protectant Uses
  6. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
41250-642
Proprietary Name:
Meijer Oatmeal Bath Skin Protectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Meijer Distribution, Inc
Labeler Code:
41250
Product Label ID:
ae8ba5c8-5c32-4f23-b8eb-9f4d0eeb9adc
Start Marketing Date: [9]
07-26-2011
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GRAY (C48324)

Product Packages

NDC Code 41250-642-01

Package Description: 8 PACKET in 1 CARTON / 42 g in 1 PACKET

Product Details

What is NDC 41250-642?

The NDC code 41250-642 is assigned by the FDA to the product Meijer Oatmeal Bath Skin Protectant which is product labeled by Meijer Distribution, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41250-642-01 8 packet in 1 carton / 42 g in 1 packet. 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 Meijer Oatmeal Bath Skin Protectant?

♦Run water in bath tub or container at full force♦Sprinkle contents of oatmeal packet directly under the faucet into the running water♦If settling occurs at the bottom, stir the oatmeal in the water

Which are Meijer Oatmeal Bath Skin Protectant UNII Codes?

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

* 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".