71745-127 NDC - GOODEARTH ()

Drug Information

Product NDC: 71745-127

Proprietary Name: GoodEarth

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: GoodEarth Distribution LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/20/2020

Package Information

No. Package Code Package Description Billing Unit
171745-127-01250 NOT APPLICABLE in 1 PACKAGE (71745-127-01) / 250 mL in 1 NOT APPLICABLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC71745-127The 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 NAMEGoodEarthThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/20/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGoodEarth Distribution LLCName 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