![Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate 400 [iU]/g; 5 mg/g; 5000 [iU]/g Ointment, 5 g — NDC 00924-5610-00 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=e55cbf7e-c955-7f1a-e053-2a95a90a3f28&name=807709-revA_FDA.jpg)
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate 400 [iU]/g; 5 mg/g; 5000 [iU]/g Ointment, 5 g — NDC 0924-5610-00 (Billing 00924-5610-00)
by Acme United Corporation · .5 g in 1 PACKET
This is a package of 5 g of Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate 400 [iU]/g; 5 mg/g; 5000 [iU]/g Ointment from Acme United Corporation, marketed since Aug 2022 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.
NDC 00924-5610-00
🏷️ FDA NDC (as labeled)
0924-5610-00
billing pads the labeler segment with a zero
This package
Contains5 g
Pack sizes3 compare ↓
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
NDC database record
One package, one record: these facts belong to NDC 0924-5610-00 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 0924 labeler · 5610 product · 00 package
- Package marketed since
- Aug 5, 2022
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC)
- 0738743120012
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
0924-5610-00
Product NDC
0924-5610
11-digit billing NDC
00924561000
RxCUI
204602
UNII
89Y4M234ES, 057Y626693, 19371312D4
UPC
0738743120012
Application #
M004
SPL Set ID
e55cbf7e-c955-7f1a-e053-2a95a90a3f28
Established class (EPC)
Aminoglycoside Antibacterial; Polymyxin-class Antibacterial
Physiologic effect
Decreased Cell Wall Synthesis & Repair
Chemical class
Aminoglycosides; Polymyxins
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2022-08-04
Route
TOPICAL
Dosage form
OINTMENT
Substance
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Quick answers
- RxCUI (RxNorm): 204602
Why two NDCs?
The FDA registers this code as 0924-5610-00 — a 4-4-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the labeler segment → 00924-5610-00. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Other antibiotics for topical use class.
Drug family (ATC)
Other antibiotics for topical use, Other antibacterials, Antibiotics
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
📗 Our plain-language guide HelloPharmacist
- It's a first-aid antibiotic you apply to small, everyday wounds — minor cuts, scrapes, and burns — to help prevent a bacterial infection from developing. Some products also help te...
- What is this triple antibiotic ointment actually for?
- Start by cleaning the wound area. Then apply a small amount — about the size of your fingertip — directly on the area up to 1 to 3 times a day. You can cover it with a sterile band...
- Most people don't have any trouble with it. The most common reaction is a mild skin irritation, redness, itching, or swelling at the spot you applied it. If you use it often, you c...
Patient education
Supplement & herbal interactions
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
💬 Questions about Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per g | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 5, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 00924-5610-00 You're viewing this Main listing | .5 g in 1 PACKET | 2022-08-05 | — | Active |
| 00924-5610-01 0924-5610-01 | 12 PACKET in 1 CARTON / .5 g in 1 PACKET | 2022-08-05 | — | Active |
| 00924-5610-02 0924-5610-02 | 25 PACKET in 1 CARTON / .5 g in 1 PACKET | 2022-08-05 | — | Active |
Pack size FAQ
What quantity is in this package?
This package contains 5 g — .5 g in 1 packet.
How does this package differ from NDC 00924-5610-01?
Both are Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate 400 [iU]/g; 5 mg/g; 5000 [iU]/g Ointment — the drug itself is identical. This page's package is the 5 g one, while NDC 00924-5610-01 is the 12 packets package.
What NDC number is used to bill for this package of Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate 400 [iU]/g; 5 mg/g; 5000 [iU]/g Ointment?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
Therapeutic equivalents
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2022
On the market since
Aug 2022
📍
2026
Currently FDA-listed
4 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
- FDA Orange Book · refreshed Oct 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 4T6H12BN9U
Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
1 inactive ingredient listed in the exact product block matched to this NDC.
The official label also statesWhite Petrolatum
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 5, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
Manufacturer & labeler
LabelerAcme United Corporation
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code00924
First marketedAug 2022
Product typeHuman Otc Drug
Portfolio59 products on file
More NDCs from Acme United Corporation labeler code 00924
- Sting Relief Pad BENZOCAINE, ISOPROPYL ALCOHOL 60 mg/g; 600 mg/g Swab NDC 0924-5202-01
- First Aid Only Sting Relief Pad BENZOCAINE, ISOPROPYL ALCOHOL 60 mg/mL; 600 mg/mL Liquid NDC 0924-5204-01
- First Aid Only Sting Relief Benzocaine .12 g/.6mL; .006 g/.6mL Swab NDC 0924-5250-01
- First Aid Only Ammonia Inhalants .045 g/.3mL Inhalant NDC 0924-5401-01
- POVIDONE-IODINE 10 mg/mL Solution NDC 0924-5408-01
- Triple Antibiotic bacitracin zinc, neomycin sulfate, polymyxin b sulfate 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g Ointment NDC 0924-5604-00
- First Aid Only Triple Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE 400 U/g; 5 mg/g; 5000 U/g Ointment NDC 0924-5618-00
- First Aid Only Neomycin Antibiotic neomycin sulfate 3.5 mg/g Ointment NDC 0924-5620-00
- First Aid Only Hydrocortisone 1% Anti-Itch 10 mg/g Cream NDC 0924-5633-00
- Hydrocortisone 1% Anti-ItchCream 10 mg/g Cream NDC 0924-5634-00
- First Aid Only First Aid-Burn Benzalkonium Chloride, Lidocaine Hydrochloride 1.3 mg/g; 5 mg/g Cream NDC 0924-5702-00
- First Aid Only First Aid/Burn LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE 5 mg/g; 1.3 mg/g Cream NDC 0924-5730-00
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
• USES First aid to help prevent infection in minor: cuts scrapes burns
⏱️ Dosage and Administration ▾
DIRECTIONS Adults and Children Clean the affected area. Apply a small amount of product (equal to the surface area of a fingertip) 1 to 3 times daily. May be covered with a sterile bandage.
⚠️ Warnings ▾
WARNINGS For external use only DO NOT USE Do not use • in the eyes •over large areas of the body •if you are allergic to any of the ingredients •longer than 1 week unless directed by a doctor •on deep lacerations or puncture wounds, animal bites, or serious burns STOP USE AND ASK A DOCTOR IF •condition persists or gets worse •a rash or allergic reaction occurs •condition persists for more than 7 days Keep out the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
📦 Storage and Handling ▾
OTHER INFORMATION Store at 15°- 30°C (59°- 86°F)
🧪 Active Ingredient ▾
• ACTIVE INGREDIENT Bacitracin zinc 400 units Neomycin sulfate 5 mg (equivalent to 3.5 mg. of neomycin base) Polymyxin - B sulfate 5000 units Active ingredient (in each gram) Purpose Bacitracin Zinc 400 Units First Aid Antibiotic Neomycin Sulfate 5mg (Equivalent to 3.5 mg of Neomycin base) First Aid Antibiotic Polymyxin B Sulfate 5000 Units First Aid Antibiotic
🧪 Inactive Ingredients ▾
INACTIVE INGREDIENT White Petrolatum
🎯 Purpose ▾
Active ingredient (in each gram) Purpose Bacitracin Zinc 400 Units First Aid Antibiotic Neomycin Sulfate 5mg (Equivalent to 3.5 mg of Neomycin base) First Aid Antibiotic Polymyxin B Sulfate 5000 Units First Aid Antibiotic
📄 Do Not Use ▾
DO NOT USE Do not use • in the eyes •over large areas of the body •if you are allergic to any of the ingredients •longer than 1 week unless directed by a doctor •on deep lacerations or puncture wounds, animal bites, or serious burns
📄 Stop Use and Ask a Doctor If ▾
STOP USE AND ASK A DOCTOR IF •condition persists or gets worse •a rash or allergic reaction occurs •condition persists for more than 7 days
📄 Keep Out of Reach of Children ▾
Keep out the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
📄 Questions or Comments ▾
Questions 1.800.835.2263
📄 Package Label / Principal Display Panel ▾
Carton Image Carton Image
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
About this NDC listing & data coverage
Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Acme United Corporation. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 12 packets (00924-5610-01), 25 packets (00924-5610-02). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Acme United Corporation is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.