NDC Package 84010-213-01 Lumumu Toenail Repair Pen

Undecylenic Acid 25% Toenail Repair Pen Liquid Topical - 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:
84010-213-01
Package Description:
12 mL in 1 BOX
Product Code:
Proprietary Name:
Lumumu Toenail Repair Pen
Non-Proprietary Name:
Undecylenic Acid 25% Toenail Repair Pen
Substance Name:
Undecylenic Acid
Usage Information:
For athlete's foot and ringworm : use daily for 4 weeks. Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise child ren in the use of this product. This product is not effective for the treatment of ringworm of the scalp or nails. For athlete's foot: pay special attention to spaces between the toes, wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. To prevent athlete's foot, apply once or twice daily (morning and/or night). Apply to skin around the nail and cuticle.
11-Digit NDC Billing Format:
84010021301
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Jiangxi Hemei Pharmaceutical Co., Ltd
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):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
M005
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
11-04-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N

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 84010-213-01?

The NDC Packaged Code 84010-213-01 is assigned to a package of 12 ml in 1 box of Lumumu Toenail Repair Pen, a human over the counter drug labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. The product's dosage form is liquid and is administered via topical form.

Is NDC 84010-213 included in the NDC Directory?

Yes, Lumumu Toenail Repair Pen with product code 84010-213 is active and included in the NDC Directory. The product was first marketed by Jiangxi Hemei Pharmaceutical Co., Ltd on November 04, 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 84010-213-01?

The 11-digit format is 84010021301. 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
5-3-284010-213-015-4-284010-0213-01