75936-135 NDC - EVERYDAY SUNSCREEN SPF 50 ()

Drug Information

Product NDC: 75936-135

Proprietary Name: Everyday Sunscreen SPF 50

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: TAYLOR JAMES, LTD.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/20/2015

Package Information

No. Package Code Package Description Billing Unit
175936-135-021 BOTTLE in 1 CARTON (75936-135-02) / 71 mL in 1 BOTTLE (75936-135-01)
275936-135-0330 mL in 1 BOTTLE (75936-135-03)
375936-135-04222 mL in 1 BOTTLE (75936-135-04)
475936-135-05532 mL in 1 BOTTLE (75936-135-05)
575936-135-063 mL in 1 PACKET (75936-135-06)
675936-135-0710 mL in 1 BOTTLE (75936-135-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75936-135The 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 50The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXSupergoopA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE1/20/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETAYLOR JAMES, LTD.Name 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