NDC 73310-5022 Face Spf 50

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:
73310-5022
Proprietary Name:
Face Spf 50
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Agefarm Srl
Labeler Code:
73310
Start Marketing Date: [9]
08-28-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - CREAM)

Product Packages

NDC Code 73310-5022-2

Package Description: 50 mL in 1 CONTAINER

Product Details

What is NDC 73310-5022?

The NDC code 73310-5022 is assigned by the FDA to the product Face Spf 50 which is product labeled by Agefarm Srl. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73310-5022-2 50 ml in 1 container . 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 Face Spf 50?

Apply liberally 15 minutes before sun exposurereapply: at least every 2 hours, immediately after towel dryinguse a water-resistant sunscreen if swimming or sweatingchildren under 6 months: Ask a doctorSun Protection Measures. Spending time in the sun increases your risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including:limite the time in the sun, especially from 10 a.m. - 2 p.m.wear long-sleeved shirts, pants, hats, and sunglasses

Which are Face Spf 50 UNII Codes?

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

Which are Face Spf 50 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".