NDC 58400-006 Anti-aging Day Protect Spf 22

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:
58400-006
Proprietary Name:
Anti-aging Day Protect Spf 22
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmco Laboratories Inc.
Labeler Code:
58400
Start Marketing Date: [9]
06-01-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 58400-006-01

Package Description: 87 g in 1 TUBE

NDC Code 58400-006-02

Package Description: 3900 g in 1 BOTTLE, PLASTIC

Product Details

What is NDC 58400-006?

The NDC code 58400-006 is assigned by the FDA to the product Anti-aging Day Protect Spf 22 which is product labeled by Pharmco Laboratories Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 58400-006-01 87 g in 1 tube , 58400-006-02 3900 g in 1 bottle, plastic . 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 Anti-aging Day Protect Spf 22?

After cleansing apply evenly to face and neck every morning, at least 15 minutes before sun exposure.Use a water resistant sunscreen if swimming or sweating.Reapply at least every 2 hours or after sweating.Children under 6 months of age: Ask a doctor. (Not intended for use on children)

Which are Anti-aging Day Protect Spf 22 UNII Codes?

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

Which are Anti-aging Day Protect Spf 22 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".