72119-005 NDC - PFA ()

Drug Information

Product NDC: 72119-005

Proprietary Name: PFA

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	BLUE SEA AEROSOL & DAILY CARE CO., LTD
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	6/4/2021

No.	Package Code	Package Description
1	72119-005-01	2 mL in 1 POUCH (72119-005-01)
2	72119-005-02	60 mL in 1 BOTTLE, PLASTIC (72119-005-02)
3	72119-005-03	500 mL in 1 BOTTLE, PUMP (72119-005-03)
4	72119-005-04	237 mL in 1 BOTTLE, PUMP (72119-005-04)
5	72119-005-05	375 mL in 1 BOTTLE, PUMP (72119-005-05)
6	72119-005-06	80 mL in 1 BOTTLE, PLASTIC (72119-005-06)
7	72119-005-07	100 mL in 1 BOTTLE, PLASTIC (72119-005-07)

Field Name	Field Value	Definition
PRODUCT NDC	72119-005	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	PFA	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	6/4/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	BLUE SEA AEROSOL & DAILY CARE CO., LTD	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