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  4. NDC Product Code: 58133-111 Homeopathic Lip Balm

NDC 58133-111 Homeopathic Lip Balm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58133-111?
  4. Homeopathic Lip Balm 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:
58133-111
Proprietary Name:
Homeopathic Lip Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cosmetic Specialty Labs, Inc.
Labeler Code:
58133
Product Label ID:
62478131-4ed7-5407-e053-2991aa0a5aac
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 58133-111?

The NDC code 58133-111 is assigned by the FDA to the product Homeopathic Lip Balm which is product labeled by Cosmetic Specialty Labs, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 58133-111-01 5.5 g in 1 tube , 58133-111-05 15 g in 1 jar . 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 Homeopathic Lip Balm?

Apply to affected area 2 times daily or as needed.

Which are Homeopathic Lip Balm UNII Codes?

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

Which are Homeopathic Lip Balm 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".