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  5. NDC Package Code: 85212-0006-1 Qidila Whitening Skin Lightening Cream

NDC Package 85212-0006-1 Qidila Whitening Skin Lightening Cream

Butylene Glycol, Butyrospermum Parkii (shea Butter), Kyounin Yu, Tocopherol, Ascorbic - 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:
85212-0006-1
Package Description:
30 mL in 1 BOTTLE
Product Code:
85212-0006
Proprietary Name:
Qidila Whitening Skin Lightening Cream
Non-Proprietary Name:
Butylene Glycol, Butyrospermum Parkii (shea Butter), Kyounin Yu, Tocopherol, Ascorbic Acid, Niacinamide
Substance Name:
Ascorbic Acid; Butylene Glycol; Butyrospermum Parkii (shea) Butter; Niacinamide; Prunus Armeniaca (apricot) Kernel Extract; Tocopherol
Usage Information:
This product is used as Whitening Anti-wrinkle Moisturizing Nourishing Anti-aging . 1 .Clean and dry your skin. 2 . Apply a proper amount of the cream on desired area with your fingers, using a circular motion to massage the cream into the skin. 3 .Please apply it twice a day(morning and evening)
11-Digit NDC Billing Format:
85212000601
Product Type:
Human Otc Drug
Labeler Name:
Beijing Junge Technology Co., Ltd.
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Extracorporeal - Administration outside of the body.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
505G(a)(3)
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-01-2025
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 85212-0006-1?

The NDC Packaged Code 85212-0006-1 is assigned to a package of 30 ml in 1 bottle of Qidila Whitening Skin Lightening Cream, a human over the counter drug labeled by Beijing Junge Technology Co., Ltd.. The product's dosage form is cream and is administered via extracorporeal form.

Is NDC 85212-0006 included in the NDC Directory?

Yes, Qidila Whitening Skin Lightening Cream with product code 85212-0006 is active and included in the NDC Directory. The product was first marketed by Beijing Junge Technology Co., Ltd. on January 01, 2025 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 85212-0006-1?

The 11-digit format is 85212000601. 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
5-4-185212-0006-15-4-285212-0006-01