NDC 52554-1116 Perfect Shield Rejuve Sunscreen 100

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:
52554-1116
Proprietary Name:
Perfect Shield Rejuve Sunscreen 100
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cms Lab Inc
Labeler Code:
52554
Start Marketing Date: [9]
05-30-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 52554-1116-2

Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE (52554-1116-1)

Product Details

What is NDC 52554-1116?

The NDC code 52554-1116 is assigned by the FDA to the product Perfect Shield Rejuve Sunscreen 100 which is product labeled by Cms Lab Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52554-1116-2 1 tube in 1 carton / 50 ml in 1 tube (52554-1116-1). 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 Perfect Shield Rejuve Sunscreen 100?

Apply the adequate amount onto the entire face at the last stage of your skin care routine. Re-apply frequently and generously to maintain protection. Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating. Children under 6 months of age: ask a doctor

Which are Perfect Shield Rejuve Sunscreen 100 UNII Codes?

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

Which are Perfect Shield Rejuve Sunscreen 100 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".