NDC Package 84673-003-03 Whitening

Ojw Brightening Serum Emulsion Auricular (otic); Buccal; Conjunctival; Cutaneous - View Billable Units, 11-Digit Format, RxNorm

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:
84673-003-03
Package Description:
100 mg in 1 BOTTLE
Product Code:
Proprietary Name:
Whitening
Non-Proprietary Name:
Ojw Brightening Serum
Substance Name:
3-o-ethyl Ascorbic Acid; Niacinamide
Usage Information:
HOW TO USE :After cleansing the skin in the morning and evening, apply an appropriate amount of essence evenly to the face and massage it to absorb.
11-Digit NDC Billing Format:
84673000303
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Meiya Cosmetics Co.. Ltd.
Dosage Form:
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
Administration Route(s):
  • Auricular (otic) - Administration to or by way of the ear.
  • Buccal - Administration directed toward the cheek, generally from within the mouth.
  • Conjunctival - Administration to the conjunctiva, the delicate membrane that lines the eyelids and covers the exposed surface of the eyeball.
  • Cutaneous - Administration to the skin.
Sample Package:
No
FDA Application Number:
505G(a)(3)
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
04-16-2024
End Marketing Date:
04-16-2027
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.

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Frequently Asked Questions

What is NDC 84673-003-03?

The NDC Packaged Code 84673-003-03 is assigned to a package of 100 mg in 1 bottle of Whitening, a human over the counter drug labeled by Guangzhou Meiya Cosmetics Co.. Ltd.. The product's dosage form is emulsion and is administered via auricular (otic); buccal; conjunctival; cutaneous form.

Is NDC 84673-003 included in the NDC Directory?

Yes, Whitening with product code 84673-003 is active and included in the NDC Directory. The product was first marketed by Guangzhou Meiya Cosmetics Co.. Ltd. on April 16, 2024.

What is the 11-digit format for NDC 84673-003-03?

The 11-digit format is 84673000303. 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
5-3-284673-003-035-4-284673-0003-03