NDC 0363-2120 Walgreens Earache Drops

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:
0363-2120
Proprietary Name:
Walgreens Earache Drops
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
0363
Start Marketing Date: [9]
02-10-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 0363-2120?

The NDC code 0363-2120 is assigned by the FDA to the product Walgreens Earache Drops which is product labeled by Walgreens Co. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-2120-42 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper. 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 Walgreens Earache Drops?

Adults and children over the age of 2 years :  For use in the ear only Remove any hearing aids before using this productUse 3 to 5 drops twice per day or as needed Warm the content to body temperature by holding in your handsTilt head sideways and let solution drip into ear.Tip of applicator should not enter ear canal. Keep drops in ear for 1 to 2 minutes by keeping head tilted or placing cotton in the ear. 

Which are Walgreens Earache Drops UNII Codes?

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

Which are Walgreens Earache Drops 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".