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  5. NDC Package Code: 73399-002-30 Formula 2

NDC Package 73399-002-30 Formula 2

Agnus Castus,Alpha Lipoicum Acidum,Androsterone 1 Dhea,Calcarea Carbonica, Cinchona - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
73399-002-30
Package Description:
30 mL in 1 BOTTLE
Product Code:
73399-002
Proprietary Name:
Formula 2
Non-Proprietary Name:
Agnus Castus, Alpha Lipoicum Acidum, Androsterone 1 Dhea, Calcarea Carbonica, Cinchona Officinalis, Cynara Scolymus, Dopamine Hydrochloride, Hydrastis Canadensis, Lycopodium Clavatum, Oxytocin Acetate, Quercetin, Sarcolacticum, Serotonin, Ignatia Amara, Tiliroside, Ubiquinone, Valeriana Officinalis,
Substance Name:
Alpha Lipoic Acid; Androsterone; Chaste Tree Fruit; Cinchona Officinalis Bark; Cynara Scolymus Leaf; Goldenseal; Lactic Acid, L-; Lycopodium Clavatum Spore; Oyster Shell Calcium Carbonate, Crude; Quercetin; Serotonin; Strychnos Ignatii Seed; Tiliroside; Ubidecarenone; Valerian
11-Digit NDC Billing Format:
73399000230
Product Type:
Human Otc Drug
Labeler Name:
20lighter, Llc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
01-30-2020
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 73399-002-30?

The NDC Packaged Code 73399-002-30 is assigned to a package of 30 ml in 1 bottle of Formula 2, a human over the counter drug labeled by 20lighter, Llc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 73399-002 included in the NDC Directory?

Yes, Formula 2 with product code 73399-002 is active and included in the NDC Directory. The product was first marketed by 20lighter, Llc. on January 30, 2020 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 73399-002-30?

The 11-digit format is 73399000230. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-273399-002-305-4-273399-0002-30