NDC 61715-030 Broad Spectrum Spf 70 Sunscreen Preferred Plus Pharmacy

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:
61715-030
Proprietary Name:
Broad Spectrum Spf 70 Sunscreen Preferred Plus Pharmacy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kinray Inc.
Labeler Code:
61715
Start Marketing Date: [9]
03-15-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61715-030-06

Package Description: 177 mL in 1 CAN

Product Details

What is NDC 61715-030?

The NDC code 61715-030 is assigned by the FDA to the product Broad Spectrum Spf 70 Sunscreen Preferred Plus Pharmacy which is product labeled by Kinray Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61715-030-06 177 ml in 1 can . 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 Broad Spectrum Spf 70 Sunscreen Preferred Plus Pharmacy?

UsesHelps prevent sunburn.

Which are Broad Spectrum Spf 70 Sunscreen Preferred Plus Pharmacy UNII Codes?

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

Which are Broad Spectrum Spf 70 Sunscreen Preferred Plus Pharmacy 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".