61619-866 NDC - PRO-TECT SUNSCREEN FOR PROFESSIONALS ()

Drug Information

Product NDC: 61619-866

Proprietary Name: Pro-Tect Sunscreen for Professionals

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	61619-866-01	29.6 mL in 1 BOTTLE, PLASTIC (61619-866-01)
2	61619-866-02	59.1 mL in 1 BOTTLE, PLASTIC (61619-866-02)
3	61619-866-04	118.3 mL in 1 BOTTLE, PLASTIC (61619-866-04)
4	61619-866-08	236.6 mL in 1 BOTTLE, PLASTIC (61619-866-08)
5	61619-866-32	946.4 mL in 1 BOTTLE, PLASTIC (61619-866-32)

Field Name	Field Value	Definition
PRODUCT NDC	61619-866	The 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 NAME	Pro-Tect Sunscreen for Professionals	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	2/8/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	A-Cute Derm, Incorporated	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