72636-100 NDC - PERILLA FO TI ()

Drug Information

Product NDC: 72636-100

Proprietary Name: Perilla Fo ti

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: The Greenery Lab
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/31/2018

Package Information

No. Package Code Package Description Billing Unit
172636-100-021 BOTTLE, PUMP in 1 BOX (72636-100-02) / 500 g in 1 BOTTLE, PUMP (72636-100-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72636-100The 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 NAMEPerilla Fo tiThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/31/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEThe Greenery LabName 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