NDC 58411-257 Shiseido Protective Lip Conditioner

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:
Proprietary Name:
Shiseido Protective Lip Conditioner
Product Type: [3]
Labeler Name: [5]
Shiseido Americas Corporation
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Packages

NDC Code 58411-257-20

Package Description: 1 CARTRIDGE in 1 CARTON / 4 g in 1 CARTRIDGE

Product Details

What is NDC 58411-257?

The NDC code 58411-257 is assigned by the FDA to the product Shiseido Protective Lip Conditioner which is product labeled by Shiseido Americas Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58411-257-20 1 cartridge in 1 carton / 4 g in 1 cartridge. 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 Shiseido Protective Lip Conditioner?

For sunscreen use:apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hourschildren under 6 months: Ask a doctor

Which are Shiseido Protective Lip Conditioner UNII Codes?

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

Which are Shiseido Protective Lip Conditioner 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".