72566-051 NDC - SUNNYLIFE SPF 50 SUNSCREEN COCONUT SCENTED ()

Drug Information

Product NDC: 72566-051

Proprietary Name: SUNNYLIFE SPF 50 SUNSCREEN COCONUT SCENTED

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: OUTLIVING PTY LTD
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/6/2019

Package Information

No. Package Code Package Description Billing Unit
172566-051-06200 mL in 1 BOTTLE (72566-051-06)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72566-051The 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 NAMESUNNYLIFE SPF 50 SUNSCREEN COCONUT SCENTEDThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/6/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOUTLIVING PTY LTDName 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