NDC 0096-0721 Daily Facial Moisturizer Spf 25

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:
0096-0721
Proprietary Name:
Daily Facial Moisturizer Spf 25
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Person And Covey
Labeler Code:
0096
Start Marketing Date: [9]
08-01-1991
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0096-0721-07

Package Description: 7 g in 1 BOTTLE

NDC Code 0096-0721-45

Package Description: 45 g in 1 BOTTLE

Price per Unit: $0.20431 per GM

Product Details

What is NDC 0096-0721?

The NDC code 0096-0721 is assigned by the FDA to the product Daily Facial Moisturizer Spf 25 which is product labeled by Person And Covey. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 0096-0721-07 7 g in 1 bottle , 0096-0721-45 45 g in 1 bottle . 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 Daily Facial Moisturizer Spf 25?

-Apply DML Daily Facial Moisturizer liberally and evenly 15-20 minutes before sun exposure and message in gently, allowing it to dry. Reapply as needed or as directed by your Dermatologist.-DML Daily Facial is an excellant make-up base.

Which are Daily Facial Moisturizer Spf 25 UNII Codes?

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

Which are Daily Facial Moisturizer Spf 25 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".