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55789-2901 NDC - SPF 16 BRIGHTENING ()

Drug Information

Product NDC: 55789-2901

Proprietary Name: SPF 16 BRIGHTENING

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Mineral Fusion Natural Brands
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/1/2014

Package Information

No. Package Code Package Description Billing Unit
155789-2901-11 TUBE in 1 CARTON (55789-2901-1) / 28 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC55789-2901The 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 NAMESPF 16 BRIGHTENINGThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/1/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMineral Fusion Natural BrandsName 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