What is NDC 80489-919?

80489-919 is the product NDC for Drs. Pharmacy Triple Antibiotic AND BURN RELIEF, Bacitracin zinc 500 [USP'U]/1000mg + 3 more ingredients ointment, listed with the FDA by OL PHARMA TECH, LLC Drs PHARMACY. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Drs. Pharmacy Triple Antibiotic AND BURN RELIEF (Bacitracin zinc, neomycin sulfate, polymyxin b sulfate).

What is the active ingredient?

Bacitracin zinc, Neomycin sulfate, Polymyxin b sulfate, Pramoxine hydrochloride.

OL PHARMA TECH, LLC Drs PHARMACY, NDC labeler code 80489. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Drs. Pharmacy Triple Antibiotic AND BURN RELIEF?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

NDC 80489-919

NDC codes

FDA NDC Directory

Product NDC (as listed)80489-919Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80489-0919Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
80489-919-01	8048909190180489091901	1 TUBE in 1 CARTON (80489-919-01) / 14000 mg in 1 TUBEMarketed from Sep 5, 2021
80489-919-02	8048909190280489091902	1 TUBE in 1 CARTON (80489-919-02) / 28300 mg in 1 TUBEMarketed from Sep 5, 2021

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Drs. Pharmacy Triple Antibiotic AND BURN RELIEF
Generic name (nonproprietary): bacitracin zinc, neomycin sulfate, polymyxin b sulfate
Active ingredients: Bacitracin zinc — 500 [USP'U]/1000mgNeomycin sulfate — 3.5 mg/1000mgPolymyxin b sulfate — 10000 [USP'U]/1000mgPramoxine hydrochloride — 10 mg/1000mg
Dosage form: Ointment
Route: Topical
Labeler: OL PHARMA TECH, LLC Drs PHARMACYNDC labeler code 80489
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 003
Marketing start: Sep 5, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Aminoglycosides (Chemical structure)Decreased Cell Wall Synthesis & Repair (Physiologic effect)Polymyxins (Chemical structure)
Identifiers: Product ID 80489-919_4928d0c5-0313-dfd6-e063-6394a90ab798SPL ID 4928d0c5-0313-dfd6-e063-6394a90ab798SPL set ID 4928d9dd-542b-fe8b-e063-6294a90a9252RxCUI 1359350UNII 89Y4M234ES, 057Y626693, 19371312D4, 88AYB867L5
Pharmacologic class: Aminoglycoside Antibacterial; Polymyxin-class Antibacterial

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N480489091901 followed by a unit qualifier and the quantity

Package 80489-0919-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 22, 2026.

Indications (excerpt from the label)

Uses first aid to help prevent infection in minor • cuts • scrapes • burns

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80489-919

What is NDC 80489-919?: 80489-919 is the product NDC for Drs. Pharmacy Triple Antibiotic AND BURN RELIEF, Bacitracin zinc 500 [USP'U]/1000mg + 3 more ingredients ointment, listed with the FDA by OL PHARMA TECH, LLC Drs PHARMACY. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Drs. Pharmacy Triple Antibiotic AND BURN RELIEF (Bacitracin zinc, neomycin sulfate, polymyxin b sulfate).
What is the active ingredient?: Bacitracin zinc, Neomycin sulfate, Polymyxin b sulfate, Pramoxine hydrochloride.
Who is the labeler?: OL PHARMA TECH, LLC Drs PHARMACY, NDC labeler code 80489. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Drs. Pharmacy Triple Antibiotic AND BURN RELIEF?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under M 003

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 003
Product	Strength	Form · route	Labeler	Product NDC
Antisepticethanol	Alcohol .62 mL/mL	GelTopical	McKesson	68599-5322
Hand sanitizer 16.9oz with vitamin Eethyl alcohol 70%	Alcohol 70 mL/100mL	LiquidTopical	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	75742-021
Mistify Pina Colada Hand Sanitezeralcohol antiseptic	Alcohol 62 mL/100mL	LiquidTopical	Kingkey MBC Life Technology Group Co.,Ltd	73928-178
Solar Flare Hand Sanitizer Sunset Sambaalcohol	Alcohol 62 mL/100mL	SprayTopical	Scent Theory Products LLC	76891-153
Klean Freakbenzalkonium chloride	Benzalkonium chloride .13 g/100g	ClothTopical	KLEAN FREAK, LLC	78982-005
Guardellebenzalkonium chloride	Benzalkonium chloride .13 g/100mL	Aerosol, FoamTopical	Social Medical Supply LLC	85754-000
RITE AID Maximum strength pain relievingbenzalkonium chloride and lidocaine hydrochloride	Benzalkonium chloride .13 g/100mL; Lidocaine hydrochloride 4 g/100mL	LiquidTopical	RITE AID	11822-7220
Hand Sanitizer	Alcohol 70 mL/100mL	GelExtracorporeal	Zhejiang Meimi Technology Co., Ltd.	41366-055
Smart Care Cucumber Melon Hand Sanitizeralcohol	Alcohol 70 mL/100mL	SprayTopical	Shenzhen Lantern Scicence Co.,Ltd.	54860-509
Walgreen Maximum strength pain relieving cleansingbenzalkonium chloride and lidocaine hydrochloride	Benzalkonium chloride .13 g/100mL; Lidocaine hydrochloride 4 g/100mL	LiquidTopical	WALGREENS CO.	0363-7020
American Red Cross 70% Ethyl Alcohol Hand Sanitizerethyl alcohol	Alcohol 70 mL/100mL	GelTopical	Zhejiang Guoyao Jingyue Aerosol Co., Ltd	75742-018
Thompson Burn Cream with Lidocainebenzalkonium chloride, lidocaine	Lidocaine hydrochloride 5 mg/g; Benzalkonium chloride 1.3 mg/g	CreamTopical	Thompson Safety	73408-160
Scentfull Hand Sanitizer Whipped Coconutalcohol	Alcohol 62 mL/100mL	SprayTopical	Scent Theory Products LLC	76891-150
Klean Freakbenzalkonium chloride	Benzalkonium chloride .13 g/100g	ClothTopical	KLEAN FREAK, LLC	78982-002
Hand Sanitizeralcohol 62%	Alcohol .62 g/g	GelTopical	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	87910-009
Obstetrical Towelettebenzalkonium chloride	Benzalkonium chloride 1.3 mg/g	ClothTopical	Jianerkang Medical Co., Ltd	34645-0015
Hand Sanitizer	Alcohol 70 mL/100mL	GelExtracorporeal	Zhejiang Meimi Technology Co., Ltd.	41366-052
Ashley Belle 1 oz., Moisturizing Hand Sanitizing, Hibiscus Nectarethyl alcohol	Alcohol 70 mL/100mL	SprayTopical	MY IMPORTS USA LLC	51628-4563
Soft Touch Plus Antibacterial Hand Item 1039chloroxylenol	Chloroxylenol .3 g/100mL	SoapTopical	AMERICAN CHEMICAL AND SANITARY SUPPLY INC	50536-139
Hydrogen Peroxide	Hydrogen peroxide 30 mg/mL	SolutionTopical	Perrigo Direct, Inc	50804-871

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Drs. Pharmacy Triple Antibiotic AND BURN RELIEF NDC 80489-919