52554-1200 NDC - CELL FUSION C LASER SUNSCREEN ()

Drug Information

Product NDC: 52554-1200

Proprietary Name: Cell Fusion C Laser Sunscreen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: CMS LAB Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2020

Package Information

No. Package Code Package Description Billing Unit
152554-1200-110 mL in 1 CARTON (52554-1200-1)
252554-1200-250 mL in 1 CARTON (52554-1200-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC52554-1200The 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 NAMECell Fusion C Laser 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 DATE5/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECMS LAB 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