NDC 71226-004 Painbloc24 Prowomen Womens Discomforts Menthol Pain And Sleep Patch

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:
71226-004
Proprietary Name:
Painbloc24 Prowomen Womens Discomforts Menthol Pain And Sleep Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
71226
Start Marketing Date: [9]
01-25-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 71226-004?

The NDC code 71226-004 is assigned by the FDA to the product Painbloc24 Prowomen Womens Discomforts Menthol Pain And Sleep Patch which is product labeled by Vizuri Health Sciences Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71226-004-01 1 pouch in 1 carton / 5 patch in 1 pouch. 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 Painbloc24 Prowomen Womens Discomforts Menthol Pain And Sleep Patch?

Adults over 18 years:clean and dry affected areatrim excessive hair for better adhesionopen pouch and remove patchremove backing from patch by grasping both ends and pulling backing apartpeel off one half of backing and place patch onto affected areapeel off other half of backing and press and smooth onto skinuse patch as needed for up to 8 hours. Do not remove when wet or directly after showering or bathing. Allow patch to dry and then slowly remove.use one patch at a time for up to 8 hoursChildren under 18 years: consult a doctor

Which are Painbloc24 Prowomen Womens Discomforts Menthol Pain And Sleep Patch UNII Codes?

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

Which are Painbloc24 Prowomen Womens Discomforts Menthol Pain And Sleep Patch 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".