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  4. NDC Product Code: 80554-002 Biorlx Lip Balm Collagen

NDC 80554-002 Biorlx Lip Balm Collagen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80554-002?
  4. Biorlx Lip Balm Collagen 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:
80554-002
Proprietary Name:
Biorlx Lip Balm Collagen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lotusa Llc.
Labeler Code:
80554
Product Label ID:
af99febf-b536-3038-e053-2a95a90a641d
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80554-002-02

Package Description: 12 APPLICATOR in 1 BOX / 3.5 g in 1 APPLICATOR (80554-002-01)

Product Details

What is NDC 80554-002?

The NDC code 80554-002 is assigned by the FDA to the product Biorlx Lip Balm Collagen which is product labeled by Lotusa Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80554-002-02 12 applicator in 1 box / 3.5 g in 1 applicator (80554-002-01). 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 Biorlx Lip Balm Collagen?

Apply as needed. Apply liberally 15 minutes before sun exposure. Reapply after 60 minutes of swimming or sweatig, immediately after towel drying at leaft every 2 hours. For best results use daily.

Which are Biorlx Lip Balm Collagen UNII Codes?

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

Which are Biorlx Lip Balm Collagen 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".