NDC 61577-7505 Sore No More Plus Cbd 500mg Cool Therapy

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:
61577-7505
Proprietary Name:
Sore No More Plus Cbd 500mg Cool Therapy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sombra Cosmetics Inc.
Labeler Code:
61577
Start Marketing Date: [9]
05-23-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61577-7505-2

Package Description: 56.7 g in 1 JAR

NDC Code 61577-7505-4

Package Description: 113.4 g in 1 JAR

Product Details

What is NDC 61577-7505?

The NDC code 61577-7505 is assigned by the FDA to the product Sore No More Plus Cbd 500mg Cool Therapy which is product labeled by Sombra Cosmetics Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 61577-7505-2 56.7 g in 1 jar , 61577-7505-4 113.4 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 Sore No More Plus Cbd 500mg Cool Therapy?

Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily, rub in thoroughly until gel is absorbed, children under 2 years of age: consult a doctor.

Which are Sore No More Plus Cbd 500mg Cool Therapy UNII Codes?

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

Which are Sore No More Plus Cbd 500mg Cool Therapy 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:

* Please review the disclaimer below.

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".