NDC 73191-125 Jouvalle Deep Nourishing Luminosity Day

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:
73191-125
Proprietary Name:
Jouvalle Deep Nourishing Luminosity Day
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
73191
Start Marketing Date: [9]
08-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 73191-125?

The NDC code 73191-125 is assigned by the FDA to the product Jouvalle Deep Nourishing Luminosity Day which is product labeled by Florida Private Labeling Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73191-125-19 1 jar in 1 carton / 50 g in 1 jar. 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 Jouvalle Deep Nourishing Luminosity Day?

•After cleansing, apply liberally and evenly 15 minutes before sun exposure. Smooth over face and neck and chest daily for optimal results.•Reapply at least every two (2) hours.•Use water resistant sunscreen if swimming or sweating.Sun 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 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 sunglassesFor children under 6 months of age: Ask doctor.

Which are Jouvalle Deep Nourishing Luminosity Day UNII Codes?

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

Which are Jouvalle Deep Nourishing Luminosity Day 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:

* Please review the disclaimer below.

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".