NDC 62721-8127 Lypsyl Vanilla Plum Intense Protection

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:
Lypsyl Vanilla Plum Intense Protection
Product Type: [3]
Labeler Name: [5]
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Characteristics


Product Packages

NDC Code 62721-8127-8

Package Description: 2.83 CANISTER in 1 BLISTER PACK / 2.83 g in 1 CANISTER (62721-8127-6)

Product Details

What is NDC 62721-8127?

The NDC code 62721-8127 is assigned by the FDA to the product Lypsyl Vanilla Plum Intense Protection which is product labeled by Lornamead. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62721-8127-8 2.83 canister in 1 blister pack / 2.83 g in 1 canister (62721-8127-6). 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 Lypsyl Vanilla Plum Intense Protection?

Apply liberally 15 minutes before sun exposureafter 40 minutes of swimming or sweatingat least every 2 hourschildren under 6 months: ask a doctorSun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with Broad Spectrum SPF vlaue of 15 or higher and other sun protection measures includinglimit time in the sun, especially from 10a.m. -2 p.m.wear long-sleeved shirts, pants hats and sunglasses

Which are Lypsyl Vanilla Plum Intense Protection UNII Codes?

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

Which are Lypsyl Vanilla Plum Intense Protection 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".