81535-203 NDC - FLAWLESS BRIGHTENING SUNSCREEN ()

Drug Information

Product NDC: 81535-203

Proprietary Name: Flawless Brightening Sunscreen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Flawless Skin Care LLC (dba Abby Skin Clinic)
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/1/2021

Package Information

No. Package Code Package Description Billing Unit
181535-203-5053 g in 1 BOTTLE, PUMP (81535-203-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC81535-203The 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 NAMEFlawless Brightening SunscreenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEFlawless Skin Care LLC (dba Abby Skin Clinic)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