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  5. NDC Package Code: 84449-003-01 Sting Relief Prep Pad

NDC Package 84449-003-01 Sting Relief Prep Pad

Patch Topical - 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:
84449-003-01
Package Description:
1 g in 1 PATCH
Product Code:
84449-003
Proprietary Name:
Sting Relief Prep Pad
Non-Proprietary Name:
Sting Relief Prep Pad
Substance Name:
Aloe; Benzocaine; Citronella Oil; Glycerin; Lanolin
Usage Information:
Mainly used for wiping before mosquito bites and cleaning and disinfecting after being bitten by mosquitoes
11-Digit NDC Billing Format:
84449000301
Product Type:
Human Otc Drug
Labeler Name:
Shenzhen Benliju Bio-tech Co.,ltd
Dosage Form:
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
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):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M003
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-20-2024
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 84449-003-01?

The NDC Packaged Code 84449-003-01 is assigned to a package of 1 g in 1 patch of Sting Relief Prep Pad, a human over the counter drug labeled by Shenzhen Benliju Bio-tech Co.,ltd. The product's dosage form is patch and is administered via topical form.

Is NDC 84449-003 included in the NDC Directory?

Yes, Sting Relief Prep Pad with product code 84449-003 is active and included in the NDC Directory. The product was first marketed by Shenzhen Benliju Bio-tech Co.,ltd on August 20, 2024 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 84449-003-01?

The 11-digit format is 84449000301. 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
5-3-284449-003-015-4-284449-0003-01