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  4. NDC Product Code: 60512-9086 Kids Relief Arnica

NDC 60512-9086 Kids Relief Arnica

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60512-9086?
  4. Kids Relief Arnica 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:
60512-9086
Proprietary Name:
Kids Relief Arnica
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Homeolab Usa Inc
Labeler Code:
60512
Product Label ID:
e2147c5d-8317-4223-8a23-c1c7df86448e
Start Marketing Date: [9]
03-15-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 60512-9086?

The NDC code 60512-9086 is assigned by the FDA to the product Kids Relief Arnica which is product labeled by Homeolab Usa Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 60512-9086-1 1 tube in 1 carton / 50 g in 1 tube, 60512-9086-2 6 g in 1 tube . 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 Arnica?

- Apply a thin layer to the affected area, rub in gently. Repeat 3 times a day or as needed.- Children under 2 yrs: ask a doctor.

Which are Kids Relief Arnica UNII Codes?

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

Which are Kids Relief Arnica 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".