75936-215 NDC - EVERYDAY SUNSCREEN SPF 50 WITH SUNFLOWER EXTRACT ()

Drug Information

Product NDC: 75936-215

Proprietary Name: EVERYDAY SUNSCREEN SPF 50 with Sunflower Extract

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Taylor James
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/19/2019

Package Information

No. Package Code Package Description Billing Unit
175936-215-01532 mL in 1 BOTTLE (75936-215-01)
275936-215-02222 mL in 1 BOTTLE (75936-215-02)
375936-215-0371 mL in 1 BOTTLE (75936-215-03)
475936-215-0430 mL in 1 BOTTLE (75936-215-04)
575936-215-0510 mL in 1 BOTTLE (75936-215-05)
675936-215-063 mL in 1 BOTTLE (75936-215-06)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75936-215The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEEVERYDAY SUNSCREEN SPF 50 with Sunflower ExtractThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/19/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETaylor JamesName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023