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  4. NDC Product Code: 60512-9214 Kids Relief Ear Relief

NDC 60512-9214 Kids Relief Ear Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 60512-9214?
  5. Kids Relief Ear Relief Uses
  6. Active Ingredients UNII Codes
  7. 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:
60512-9214
Proprietary Name:
Kids Relief Ear Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Homeolab Usa Inc
Labeler Code:
60512
Product Label ID:
31816a46-7aff-4f96-91ec-b5c28219a397
Start Marketing Date: [9]
10-26-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)
RASPBERRY (C73413)

Product Packages

NDC Code 60512-9214-8

Package Description: 1 BOTTLE in 1 CARTON / 25 mL in 1 BOTTLE

Product Details

What is NDC 60512-9214?

The NDC code 60512-9214 is assigned by the FDA to the product Kids Relief Ear Relief which is product labeled by Homeolab Usa Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60512-9214-8 1 bottle in 1 carton / 25 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 Kids Relief Ear Relief?

Children under 6 months of age: Consult a licensed healthcare practitioner before using this product.Children 6 months to 2 years old: 0.5 ml orally every 8 hours or 3 times a day. Children 2 to 9 years old: 0.75 ml every 8 hours or 3 times a day. 

Which are Kids Relief Ear Relief UNII Codes?

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

Which are Kids Relief Ear Relief 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".