NDC Package 13709-330-02 Phenylephrine Hemorrhoidal

Hemorrhoidal Suppositories Suppository Rectal - 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:
13709-330-02
Package Description:
15 BLISTER PACK in 1 CARTON / 2 g in 1 BLISTER PACK
Product Code:
Proprietary Name:
Phenylephrine Hemorrhoidal
Non-Proprietary Name:
Hemorrhoidal Suppositories
Substance Name:
Phenylephrine Hydrochloride
Usage Information:
• Adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before insertion of this product. • Detach one suppository from the strip; remove the foil wrapper as shown in the illustration • Insert one suppository into the rectum pointed end first, up to 4 times daily, especially at night, in the morning or after each bowel movement.
11-Digit NDC Billing Format:
13709033002
NDC to RxNorm Crosswalk:
  • RxCUI: 2715398 - phenylephrine hydrochloride 0.25 % Rectal Suppository
  • RxCUI: 2715398 - phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository
Product Type:
Human Otc Drug
Labeler Name:
Neilmed Pharmaceuticals Inc.
Dosage Form:
Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
Administration Route(s):
Rectal - Administration to the rectum.
Sample Package:
No
FDA Application Number:
M015
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-23-2025
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
13709-330-0130 BLISTER PACK in 1 CARTON / 2 g in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 13709-330-02?

The NDC Packaged Code 13709-330-02 is assigned to a package of 15 blister pack in 1 carton / 2 g in 1 blister pack of Phenylephrine Hemorrhoidal, a human over the counter drug labeled by Neilmed Pharmaceuticals Inc.. The product's dosage form is suppository and is administered via rectal form.

Is NDC 13709-330 included in the NDC Directory?

Yes, Phenylephrine Hemorrhoidal with product code 13709-330 is active and included in the NDC Directory. The product was first marketed by Neilmed Pharmaceuticals Inc. on May 23, 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 13709-330-02?

The 11-digit format is 13709033002. 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
5-3-213709-330-025-4-213709-0330-02