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  4. NDC Product Code: 11822-7795 First Aid Antiseptic Rite Aid Pharmacy

NDC 11822-7795 First Aid Antiseptic Rite Aid Pharmacy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11822-7795?
  4. First Aid Antiseptic Rite Aid Pharmacy Uses
  5. Active Ingredients UNII Codes
  6. Inactive 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:
11822-7795
Proprietary Name:
First Aid Antiseptic Rite Aid Pharmacy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid
Labeler Code:
11822
Product Label ID:
7e30ce59-72fc-43c3-b451-e9d531fdbc4c
Start Marketing Date: [9]
03-29-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11822-7795-4

Package Description: 150 mL in 1 BOTTLE

Product Details

What is NDC 11822-7795?

The NDC code 11822-7795 is assigned by the FDA to the product First Aid Antiseptic Rite Aid Pharmacy which is product labeled by Rite Aid. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-7795-4 150 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 First Aid Antiseptic Rite Aid Pharmacy?

Adults and children 2 years and older: clean the affected area. Apply small amount on the area 1-3 times daily; may be covered with sterile bandage (let dry first)Children under 2 years: ask a doctor

Which are First Aid Antiseptic Rite Aid Pharmacy UNII Codes?

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

Which are First Aid Antiseptic Rite Aid Pharmacy 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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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".