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Drug Information

Product NDC: 72879-505

Proprietary Name: NON-NANO SUNSCREEN

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ProCaps Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/29/2019

Package Information

No. Package Code Package Description Billing Unit
172879-505-021 TUBE in 1 BOX (72879-505-02) / 59 mL in 1 TUBE
272879-505-041 TUBE in 1 BOX (72879-505-04) / 118 mL in 1 TUBE
372879-505-061 TUBE in 1 BOX (72879-505-06) / 177 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC72879-505The 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 NAMENON-NANO SUNSCREENThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXSPF 40A 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 DATE3/29/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEProCaps Laboratories, Inc.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