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  4. NDC Product Code: 50066-071 Teatrical Pro-aclarant Day

NDC 50066-071 Teatrical Pro-aclarant Day

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50066-071?
  5. Teatrical Pro-aclarant Day Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50066-071
Proprietary Name:
Teatrical Pro-aclarant Day
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genomma Lab Usa
Labeler Code:
50066
Product Label ID:
4f7a2e13-cd08-4b2f-b6ec-1305897f7b83
Start Marketing Date: [9]
04-22-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 50066-071-01

Package Description: 1 TUBE in 1 CARTON / 48 g in 1 TUBE

Product Details

What is NDC 50066-071?

The NDC code 50066-071 is assigned by the FDA to the product Teatrical Pro-aclarant Day which is product labeled by Genomma Lab Usa. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50066-071-01 1 tube in 1 carton / 48 g in 1 tube. 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 Teatrical Pro-aclarant Day?

This product is used as Active ingredientsPurposeAvobenzone 3.0%SunscreenOctinoxate 7.0%SunscreenOctocrylene 5.0%Sunscreen

Which are Teatrical Pro-aclarant Day UNII Codes?

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

Which are Teatrical Pro-aclarant 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:

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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".