NDC 71436-3004 Pure Cbd Hydrogel Xl With Lidocaine 4%

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:
71436-3004
Proprietary Name:
Pure Cbd Hydrogel Xl With Lidocaine 4%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
71436
Start Marketing Date: [9]
01-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 71436-3004?

The NDC code 71436-3004 is assigned by the FDA to the product Pure Cbd Hydrogel Xl With Lidocaine 4% which is product labeled by Ari Brands, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71436-3004-5 5 patch in 1 carton / 15 g in 1 patch. 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 Pure Cbd Hydrogel Xl With Lidocaine 4%?

Adults and children 12 years of age and older:Apply 1 patch to the affected area of intact skin up to 12 hours. - Clean and dry the affected area.- Open pouch and remove one patch.- Remove any protective film and apply directly to affected area of pain. Apply immediately after removal from the protective envelope. - Wash hands with soap and water after handling the patches.- Reseal pouch containing unused patches after each use. Do not store patch outside the sealed envelope. - Fold used patches so that the adhesive side sticks to itself and safely discard used patches or pieces of cut patches where children and pets cannot get to them. Children under 12 years: Ask a physician

Which are Pure Cbd Hydrogel Xl With Lidocaine 4% UNII Codes?

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

Which are Pure Cbd Hydrogel Xl With Lidocaine 4% 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".