NDC 73110-106 Sunscreen With Moisturizer Spf-30

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:
73110-106
Proprietary Name:
Sunscreen With Moisturizer Spf-30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
73110
Start Marketing Date: [9]
02-16-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 73110-106?

The NDC code 73110-106 is assigned by the FDA to the product Sunscreen With Moisturizer Spf-30 which is product labeled by Skinclinical Ai, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73110-106-11 30 ml in 1 bottle, dispensing . 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 Sunscreen With Moisturizer Spf-30?

Apply generously 15 minutes before sun exposure. Reapply after 80 minutes of swimming or sweating immediately after towel drying. Sun protection measures: Spending time in the sun increases your chances of skin cancer and early signs of aging. To decrease this risk, regularly use a sunscreen with SPF protection value 15 or higher and other sun protection measures including limited time in the sun, especially between the hours of 10am -2pm, wear long-sleeved shirt, pants, hat and sunglasses. Children under 6 months of age, consult a doctor before use.

Which are Sunscreen With Moisturizer Spf-30 UNII Codes?

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

Which are Sunscreen With Moisturizer Spf-30 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".