NDC 69065-001 Gadis Lip Moisturizer Spf15

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:
Proprietary Name:
Gadis Lip Moisturizer Spf15
Product Type: [3]
Labeler Name: [5]
Gadis Ingenious Gadgets Inc.
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Packages

NDC Code 69065-001-02

Package Description: 1.4 g in 1 CARTON

NDC Code 69065-001-04

Package Description: 2.8 g in 1 CARTON

Product Details

What is NDC 69065-001?

The NDC code 69065-001 is assigned by the FDA to the product Gadis Lip Moisturizer Spf15 which is product labeled by Gadis Ingenious Gadgets Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69065-001-02 1.4 g in 1 carton , 69065-001-04 2.8 g in 1 carton . 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 Gadis Lip Moisturizer Spf15?

Apply liberally and evenly 15 minutes before sun exposure.Sun Protection Measures.Spendingtime in the sun increases your risk of skincancer and early skin aging. To decreasethis risk, regularly use a sunscreen witha Broad Spectrum SPF value of 15 orhigher and other sun protection measuresincluding:Limit time in the sun, especially from10 a.m. – 2 p.m.Wear long-sleeved shirts, pants, hatsand sunglassesReapply:After 40 minutes swimming orsweatingImmediately after towel dryingAt least every 2 hoursChildren under 6 months of age: Aska doctor

Which are Gadis Lip Moisturizer Spf15 UNII Codes?

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

Which are Gadis Lip Moisturizer Spf15 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".