77069-002 NDC - BRITTO BODY SUNSCREEN BROAD SPECTRUM SPF 50 ()

Drug Information

Product NDC: 77069-002

Proprietary Name: Britto Body Sunscreen Broad Spectrum SPF 50

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: MR2 USA Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/15/2020

Package Information

No. Package Code Package Description Billing Unit
177069-002-01100 mL in 1 TUBE (77069-002-01)
277069-002-02200 mL in 1 TUBE (77069-002-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC77069-002The 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 NAMEBritto Body Sunscreen Broad Spectrum SPF 50The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/15/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMR2 USA CorporationName 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