81688-0650 NDC - ELEVATED ULTIMATE TINTED SUN DEFENSE BROAD SPECTRUM SPF 30 (UVA/UVB) SUNSCREEN ()

Drug Information

Product NDC: 81688-0650

Proprietary Name: Elevated Ultimate Tinted Sun Defense Broad Spectrum SPF 30 (UVA/UVB) Sunscreen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Elevated Dermatology and Skin
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2021

Package Information

No. Package Code Package Description Billing Unit
181688-0650-350 mL in 1 BOTTLE, PUMP (81688-0650-3)

NDC Record

Field Name Field Value Definition
PRODUCT NDC81688-0650The 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 NAMEElevated Ultimate Tinted Sun Defense Broad Spectrum SPF 30 (UVA/UVB) 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 DATE2/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEElevated Dermatology and SkinName 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