NDC 63645-128 Usana Lip Moisturizer

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:
63645-128
Proprietary Name:
Usana Lip Moisturizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Oralabs
Labeler Code:
63645
Start Marketing Date: [9]
07-06-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
FRUIT (C73389)

Product Packages

NDC Code 63645-128-02

Package Description: 1 LIPSTICK in 1 APPLICATOR

Product Details

What is NDC 63645-128?

The NDC code 63645-128 is assigned by the FDA to the product Usana Lip Moisturizer which is product labeled by Oralabs. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63645-128-02 1 lipstick in 1 applicator . 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 Usana Lip Moisturizer?

Apply liberally before sun exposure and as needed. 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 or higher and other sun protection measures including: limiting time in the sun (especially from 10 a.m. - 2 p.m.) and wearing long-sleeve shirts, pants, hats, and sunglasses.Children under 6 months of age: Ask a doctor before use.

Which are Usana Lip Moisturizer UNII Codes?

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

Which are Usana Lip Moisturizer 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".