NDC 0363-9021 Ear Ease

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:
0363-9021
Proprietary Name:
Ear Ease
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Company
Labeler Code:
0363
Start Marketing Date: [9]
12-14-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0363-9021-11

Package Description: 1 BOTTLE, GLASS in 1 CARTON / 10 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 0363-9021?

The NDC code 0363-9021 is assigned by the FDA to the product Ear Ease which is product labeled by Walgreen Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-9021-11 1 bottle, glass in 1 carton / 10 ml in 1 bottle, glass. 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 Ear Ease?

FOR USE IN THE EAR ONLYRemove tamper-evident seal from neck of bottle.Twist cap off bottle.Tilt head sideways.Squeeze plastic applicator and apply 4 to 5 drops in each affected ear (applicator should not enter ear canal).Keep drops in ear by keeping head tilted or placing cotton in ear.Use up to 4 times daily for no more than 48 hours, or as directed by a doctor.Children under 12 years of age consult a doctor.

Which are Ear Ease UNII Codes?

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

Which are Ear Ease 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".