NDC 70157-003 City Sunscreen Serum Broad Spectrum Spf 30 Supergoop

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:
70157-003
Proprietary Name:
City Sunscreen Serum Broad Spectrum Spf 30 Supergoop
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Baxter Laboratories
Labeler Code:
70157
Start Marketing Date: [9]
12-07-2010
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70157-003-01

Package Description: 3 mL in 1 PACKET

Product Details

What is NDC 70157-003?

The NDC code 70157-003 is assigned by the FDA to the product City Sunscreen Serum Broad Spectrum Spf 30 Supergoop which is product labeled by Baxter Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70157-003-01 3 ml in 1 packet . 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 City Sunscreen Serum Broad Spectrum Spf 30 Supergoop?

This product is used as PurposeUses Simultaneously protects skin, combats premature aging and moisturizes on contacthelps prevent sunburnIf used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging skin aging caused by the sun

Which are City Sunscreen Serum Broad Spectrum Spf 30 Supergoop UNII Codes?

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

Which are City Sunscreen Serum Broad Spectrum Spf 30 Supergoop 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".