Home › NDC Lookup › Ingredients › Bacitracin Zinc, Neomycin Sulfate And Po... › 68071-3754-01
Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g Ointment, 1 tube — NDC 68071-3754-01 package photo
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; 3.5 mg/g; 5000 [iU]/g Ointment, 1 tube — NDC 68071-3754-1 (Billing 68071-3754-01)

by NuCare Pharmaceutical, Inc. · 1 TUBE in 1 CARTON / 28.4 g in 1 TUBE

This is a package of 1 tube of Triple Antibiotic Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g Ointment from NuCare Pharmaceutical, Inc., marketed since Dec 2015 and currently FDA-listed. It is this product's only package size.

NDC 68071-3754-01
🏷️ FDA NDC (as labeled) 68071-3754-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Sep 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 68071-3754-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
68071 labeler · 3754 product · 1 package
Package marketed since
Sep 9, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0368071375411
FDA record last changed
Sep 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 68071-3754-1
Product NDC 68071-3754
11-digit billing NDC 68071375401
RxCUI 204602
UNII 89Y4M234ES, 057Y626693, 19371312D4
UPC 0368071375411
Application # M004
SPL Set ID 5b14499e-e45c-7c05-e063-6294a90a1cc2
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 2015-12-15
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 68071-3754-1 — a 5-4-1 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 package segment → 68071-3754-01. 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.

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.

Clinical

🧪 What is this product?

This is a topical antibiotic ointment containing three active ingredients: bacitracin zinc, neomycin sulfate, and polymyxin B sulfate. Each ingredient is an antibiotic commonly used to help prevent bacterial infection in minor cuts, scrapes, and wounds when applied to the skin. This is an over-the-counter monograph product, meaning it is marketed under established FDA rules for this category of topical antibiotics rather than through individual product approval.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

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 systemPer gPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
68071-3754-01 You're viewing this Main listing 1 TUBE in 1 CARTON / 28.4 g in 1 TUBE 2026-09-09 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 70677-1217-01 STRATEGIC 1 tube $0.111 — Availability likely —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 46122-0414-03 AmerisourceBergen 1 tube $0.111 — Availability likely —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 51672-2120-01 Sun 1 tube $0.139 — Availability likely —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 49035-0016-02 Wal-Mart 1 tube — — FDA listed —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 57243-0120-01 Salado 1 tube — — FDA listed —
WinCo Original Strength Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 67091-0274-28 WinCo 1 tube — — FDA listed —
Neosporin Original 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 69968-0056-01 Kenvue 1 tube — — FDA listed —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 71141-0134-32 Lidl 1 tube — — FDA listed —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 55315-0180-56 Fred's, 1 tube — — FDA listed —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 36800-0564-01 Topco 1 tube — — FDA listed —
Neosporin Original 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 69968-0634-01 Kenvue 9 g — — FDA listed —
Live Better Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/g 51143-0016-02 The 1 tube — — FDA listed —
Triple Antibiotic 400 [iU]/g; 3.5 mg/g; 5000 [iU]/gthis 68071-3754-01 NuCare 1 tube — — FDA listed —
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.

Availability & generic status

🏛️
2015
On the market since
Dec 2015
📍
2026
Currently FDA-listed
11 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.

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 H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII 512OYT1CRR
    Cocoa butter is a natural fat extracted from cocoa beans. It's used in medicines as a base for suppositories and as a lubricant to help pills dissolve smoothly.
  • UNII H3E878020N
    Cottonseed oil is a natural vegetable oil extracted from cotton plant seeds. It is used in medicines as a solvent and lubricant to help dissolve active ingredients and allow smooth tablet or capsule movement through manufacturing equipment.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • 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.
  • UNII POD38AIF08
    Sodium pyruvate is a salt form of pyruvic acid, a naturally occurring compound. It's used in medicines as a buffer to help maintain the product's pH and stability.

6 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statescocoa butter, cottonseed oil, olive oil, sodium pyruvate, vitamin E, white 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.

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

LabelerNuCare Pharmaceutical, Inc.
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code68071
First marketedDec 2015
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from NuCare Pharmaceutical, Inc. labeler code 68071

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 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 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 12 words ▾

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

⏱️ Dosage and Administration 40 words ▾

Directions clean the affected area apply 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 daily may be covered with a sterile bandage

⚠️ Warnings 87 words ▾

Warnings For external use only. Do not use if you are allergic to any of the ingredients in the eyes over large areas of the body Ask a doctor before use if you have deep or puncture wounds animal bites serious burns Stop use and ask a doctor if you need to use longer than 1 week condition persists or gets worse rash or other allergic reaction develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 31 words ▾

Other information To open: unscrew cap, pull tab to remove foil seal store at 20° to 25°C (68° to 77°F) see carton or tube crimp for lot number and expiration date

🧪 Active Ingredient 31 words ▾

Active ingredients (in each gram) Purpose Bacitracin zinc USP 400 units First aid antibiotic Neomycin sulfate USP 3.5 mg First aid antibiotic Polymyxin B sulfate USP 5,000 units First aid antibiotic

🧪 Inactive Ingredients 14 words ▾

Inactive ingredients cocoa butter, cottonseed oil, olive oil, sodium pyruvate, vitamin E, white petrolatum

🎯 Purpose 31 words ▾

Active ingredients (in each gram) Purpose Bacitracin zinc USP 400 units First aid antibiotic Neomycin sulfate USP 3.5 mg First aid antibiotic Polymyxin B sulfate USP 5,000 units First aid antibiotic

📄 Do Not Use 21 words ▾

Do not use if you are allergic to any of the ingredients in the eyes over large areas of the body

📄 Ask a Doctor Before Use If 16 words ▾

Ask a doctor before use if you have deep or puncture wounds animal bites serious burns

📄 Stop Use and Ask a Doctor If 26 words ▾

Stop use and ask a doctor if you need to use longer than 1 week condition persists or gets worse rash or other allergic reaction develops

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 3 words ▾

Questions? Call 1-866-923-4914

📄 Package Label / Principal Display Panel 9 words ▾

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton jpg

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 NuCare Pharmaceutical, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
NuCare Pharmaceutical, Inc. 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.
← 68071-3753-03 · NuCare 68071-3755-09 · NuCare →
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.