NDC 82971-010 Lapcos Suntiaging Eye Zone Cooling Golf Pat Ch S

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:
82971-010
Proprietary Name:
Lapcos Suntiaging Eye Zone Cooling Golf Pat Ch S
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
82971
Start Marketing Date: [9]
08-01-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82971-010?

The NDC code 82971-010 is assigned by the FDA to the product Lapcos Suntiaging Eye Zone Cooling Golf Pat Ch S which is product labeled by Jc Family Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82971-010-01 4 patch in 1 carton . 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 Lapcos Suntiaging Eye Zone Cooling Golf Pat Ch S?

■. Open the product to take out the patch. Remove the protection.■. Place the patch on the under-eye, cheekbone, cheek and other areas.■. Leave it for 30 minutes before removing.■. You can also use it for longer time during outdoor activities. Also suitable to use on top of sunscreen or makeup. The patch may become less adhesive when used on oily skin.

Which are Lapcos Suntiaging Eye Zone Cooling Golf Pat Ch S UNII Codes?

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

Which are Lapcos Suntiaging Eye Zone Cooling Golf Pat Ch S 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".