NDC Package 0363-2900-05 Triple Antibiotic

Bacitracin Zinc,Neomycin Sulfate,Polymyxin-b Sulfate,Pramoxine Hydrochloride Ointment - View Billable Units, 11-Digit Format, RxNorm

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:
0363-2900-05
Package Description:
1 TUBE in 1 CARTON / 14 g in 1 TUBE
Product Code:
Proprietary Name:
Triple Antibiotic
Non-Proprietary Name:
Bacitracin Zinc, Neomycin Sulfate, Polymyxin-b Sulfate, Pramoxine Hydrochloride
Substance Name:
Bacitracin Zinc; Neomycin Sulfate; Polymyxin B Sulfate; Pramoxine Hydrochloride
Usage Information:
Adults and children 2 years of age and older clean the affected areaapply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times dailymay be covered with a sterile bandagechildren under 2 years of age: ask a doctor
11-Digit NDC Billing Format:
00363290005
NDC to RxNorm Crosswalk:
  • RxCUI: 1359350 - bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG per GM Topical Ointment
  • RxCUI: 1359350 - bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 10 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical Ointment
Product Type:
Human Otc Drug
Labeler Name:
Walgreens
Dosage Form:
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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.
Sample Package:
No
FDA Application Number:
M004
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
11-27-2020
End Marketing Date:
01-27-2026
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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Frequently Asked Questions

What is NDC 0363-2900-05?

The NDC Packaged Code 0363-2900-05 is assigned to a package of 1 tube in 1 carton / 14 g in 1 tube of Triple Antibiotic, a human over the counter drug labeled by Walgreens. The product's dosage form is ointment and is administered via topical form.

Is NDC 0363-2900 included in the NDC Directory?

Yes, Triple Antibiotic with product code 0363-2900 is active and included in the NDC Directory. The product was first marketed by Walgreens on November 27, 2020.

What is the 11-digit format for NDC 0363-2900-05?

The 11-digit format is 00363290005. 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 4-4-2 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
4-4-20363-2900-055-4-200363-2900-05