NDC 54111-136 Mario Badescu Collagen Spf 15

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:
Mario Badescu Collagen Spf 15
Product Type: [3]
Labeler Name: [5]
Bentley Laboratories Llc
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Packages

NDC Code 54111-136-50

Package Description: 59 mL in 1 BOTTLE, PLASTIC

NDC Code 54111-136-51

Package Description: 29 mL in 1 PACKAGE

Product Details

What is NDC 54111-136?

The NDC code 54111-136 is assigned by the FDA to the product Mario Badescu Collagen Spf 15 which is product labeled by Bentley Laboratories Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 54111-136-50 59 ml in 1 bottle, plastic , 54111-136-51 29 ml in 1 package . 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 Mario Badescu Collagen Spf 15?

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 doctorSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:limit time in the sun, especially from 10 a.m. - 2 p.m.wear long-sleeved shirts, pants, hats, and sunglasses.

Which are Mario Badescu Collagen Spf 15 UNII Codes?

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

Which are Mario Badescu Collagen Spf 15 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".