Up And Up Suppository
NDC Package 82442-060-12

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Up And Up (phenylephrine hydrochloride) suppositories is adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. This formulation utilizes a suppository delivery system. Marketed by Target Corporation, this product is identified by NDC 82442-060 and is authorized under FDA application M015.

Identification & Billing

NDC Package Code
82442-060-12
Package Description
12 BLISTER PACK in 1 CARTON / 1 SUPPOSITORY in 1 BLISTER PACK
Product Code
82442-060
11-Digit Billing Format
82442006012

Clinical Specifications

Proprietary Name
Up And Up
Non-Proprietary Name
Phenylephrine Hydrochloride
Substance Name
Phenylephrine Hydrochloride
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
Rectal - Administration to the rectum.
Active Ingredient(s)
PHENYLEPHRINE HYDROCHLORIDE 6.25 mg/1
Pharmacologic Class
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 before inserting into the rectum as follows: hold suppository with the rounded end upcarefully separate foil tabs by inserting tip of fingernail at end marked “peel down”slowly and evenly peel apart (do not tear) foil by pulling tabs down both sides, to expose the suppositoryremove exposed suppository from the wrapperinsert one suppository into the rectum up to 4 times daily, especially at night, in the morning or after each bowel movementchildren under 12 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
Target Corporation
Product Type
Human Otc Drug
FDA Application #
M015
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-03-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 82442-060-12 identifies a specific commercial package of 12 blister pack in 1 carton / 1 suppository in 1 blister pack of Up And Up, a human over the counter drug labeled by Target Corporation. This suppository is formulated for rectal use and contains phenylephrine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Target Corporation on August 03, 2026. The current certification is valid through December 31, 2027.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82442006012. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
82442-060-12
11-Digit CMS (5-4-2)
82442-0060-12

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.