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  5. NDC Package Code: 48951-1347-3 Aquavit

NDC Package 48951-1347-3 Aquavit

Liquid Oral - 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:
48951-1347-3
Package Description:
60 mL in 1 BOTTLE, DROPPER
Product Code:
48951-1347
Proprietary Name:
Aquavit
Non-Proprietary Name:
Aquavit
Substance Name:
Ambergris; Angelica Archangelica Root; Anise; Black Pepper; Calendula Officinalis Flowering Top; Caraway Seed; Cardamom; Centaurium Erythraea Flowering Top; Chamomile; Cinnamon; Cola Nitida Seed; Coriander Oil; Equisetum Arvense Top; Fennel Seed; Ferric Oxide Red; Ferrous Arsenate; Fumaria Officinalis Flowering Top; Ginger; Gold; Honey; Hyssopus Officinalis Whole; Imperatoria Ostruthia Root; Juniper Berry; Lavandula Angustifolia Flower; Lesser Galangal Root; Litsea Cubeba Fruit; Long Pepper; Myristica Fragrans Whole; Nutmeg; Oregano; Prunus Spinosa Flower Bud; Quillaja Saponaria Bark; Rosmarinus Officinalis Flowering Top; Saffron; Sedum Roseum Whole; St. John's Wort; Sweet Marjoram; Syzygium Aromaticum Fruit; Tangerine; Thyme; Vanilla Bean; White Pepper
Usage Information:
Directions: FOR ORAL USE ONLY.
11-Digit NDC Billing Format:
48951134703
Product Type:
Human Otc Drug
Labeler Name:
Uriel Pharmacy Inc.
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):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
09-01-2009
Listing Expiration Date:
12-31-2026
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 48951-1347-3?

The NDC Packaged Code 48951-1347-3 is assigned to a package of 60 ml in 1 bottle, dropper of Aquavit, a human over the counter drug labeled by Uriel Pharmacy Inc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 48951-1347 included in the NDC Directory?

Yes, Aquavit with product code 48951-1347 is active and included in the NDC Directory. The product was first marketed by Uriel Pharmacy Inc. on September 01, 2009 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 48951-1347-3?

The 11-digit format is 48951134703. 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 5-4-1 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
5-4-148951-1347-35-4-248951-1347-03