NDC 42315-672 Moisturising Sunscreen 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:
42315-672
Proprietary Name:
Moisturising Sunscreen Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Eshu Pty Ltd
Labeler Code:
42315
Start Marketing Date: [9]
02-17-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 42315-672-02

Package Description: 1 BOTTLE in 1 BOX / 100 mL in 1 BOTTLE (42315-672-01)

Product Details

What is NDC 42315-672?

The NDC code 42315-672 is assigned by the FDA to the product Moisturising Sunscreen Spf 30 which is product labeled by Eshu Pty Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42315-672-02 1 bottle in 1 box / 100 ml in 1 bottle (42315-672-01). 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 Moisturising Sunscreen Spf 30?

-Stop use and ask a  doctor if rash or irritation occurs. -Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce risk of skin aging, skin cancer, and other harmful effects of the sun-Does not provide protection for already burnt skin-every case of sunburn damages the skin permanently -does not provide 100% protection against UV radiation-store in a cool dry place-keep carton. It contains important information

Which are Moisturising Sunscreen Spf 30 UNII Codes?

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

Which are Moisturising Sunscreen 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:

* 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".