30775-053 NDC - HELIX ()

Drug Information

Product NDC: 30775-053

Proprietary Name: Helix

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Parker Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/1/2021

Package Information

No. Package Code Package Description Billing Unit
130775-053-014 BOX in 1 CASE (30775-053-01) / 100 PACKET in 1 BOX / 3 g in 1 PACKET
230775-053-0212 TUBE in 1 BOX (30775-053-02) / 58.896 g in 1 TUBE
330775-053-0412 TUBE in 1 BOX (30775-053-04) / 117.792 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC30775-053The 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 NAMEHelixThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEParker Laboratories, Inc.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