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  5. NDC Package Code: 52380-5101-5 Aplicare Povidone-iodine Triples

NDC Package 52380-5101-5 Aplicare Povidone-iodine Triples

Povidone-iodine Solution Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
52380-5101-5
Package Description:
500 PACKET in 1 CASE / 6.5 mL in 1 PACKET
Product Code:
52380-5101
Proprietary Name:
Aplicare Povidone-iodine Triples
Non-Proprietary Name:
Povidone-iodine
Substance Name:
Povidone-iodine
Usage Information:
Apply locally as needed
11-Digit NDC Billing Format:
52380510105
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Aplicare Products, Llc
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
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):
POVIDONE-IODINE 10 mg/mL
Sample Package:
No
FDA Application Number:
part333A
Marketing Category:
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date:
05-31-2017
End Marketing Date:
11-30-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
52380-5101-1250 PACKET in 1 CASE / 6.5 mL in 1 PACKET
52380-5101-225 PACKET in 1 BOX / 6.5 mL in 1 PACKET
52380-5101-36.5 mL in 1 PACKET

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 52380-5101-5?

The NDC Packaged Code 52380-5101-5 is assigned to a package of 500 packet in 1 case / 6.5 ml in 1 packet of Aplicare Povidone-iodine Triples, a human over the counter drug labeled by Aplicare Products, Llc. The product's dosage form is solution and is administered via topical form.

Is NDC 52380-5101 included in the NDC Directory?

Yes, Aplicare Povidone-iodine Triples with product code 52380-5101 is active and included in the NDC Directory. The product was first marketed by Aplicare Products, Llc on May 31, 2017.

What is the 11-digit format for NDC 52380-5101-5?

The 11-digit format is 52380510105. 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
5-4-152380-5101-55-4-252380-5101-05