35192-013 NDC - UMBRELLA SUNSCREEN ()

Drug Information

Product NDC: 35192-013

Proprietary Name: Umbrella Sunscreen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: CA-BOTANA INTERNATIONAL
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/10/2013

Package Information

No. Package Code Package Description Billing Unit
135192-013-0250 g in 1 TUBE (35192-013-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC35192-013The 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 NAMEUmbrella 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 DATE10/10/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECA-BOTANA INTERNATIONALName 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