HomeNDC LookupIngredientsBacitracin › 59898-0720-01
Bacitracin 500 [iU]/g Ointment, 1728 packets — NDC 59898-0720-01 package photo

Bacitracin 500 [iU]/g Ointment, 1728 packets

by Water-Jel Technologies · 1728 PACKET in 1 CARTON (59898-720-01) / .9 g in 1 PACKET
NDC 59898-0720-01
🏷️ FDA NDC (as labeled) 59898-720-01 billing pads the product segment with a zero
This package
Contains1728 packets Pack sizes4 compare ↓
OTC On market Non-controlled
🗂️ Data synced Aug 6, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 59898-720-01
Product NDC 59898-720
11-digit billing NDC 59898072001
RxCUI 1366116
UNII 89Y4M234ES
UPC 0743537031443
Application # M004
SPL Set ID 412928a1-3708-4fa8-99c5-aaa2b079cf6e
Physiologic effect Decreased Cell Wall Synthesis & Repair
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2010-11-07
Route TOPICAL
Dosage form OINTMENT
Substance BACITRACIN ZINC
GCN Seq No 030028
GCN 31813
HICL code 006091
Ingredient (HICL) Bacitracin Zinc
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5W
Therapeutic class — specific (HIC3) Topical Antibiotics
AHFS code 84:04.04.00
AHFS class Antibacterials (84:04)
FDB label name BACITRACIN ZN 500 UNIT/GM OINT
FDB brand name Bacitracin Zinc
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 59898-720-01 — a 5-3-2 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 product segment → 59898-0720-01. 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.

🏭 Manufacturer & labeler

LabelerWater-Jel Technologies
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code59898
First marketedNov 2010
Product typeHuman Otc Drug
Portfolio18 products on file
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.

🩺 Clinical

Label name BACITRACIN ZN 500 UNIT/GM OINT Ingredient Bacitracin Zinc
📖 What it is MedlinePlus · NLM

Bacitracin is used to help prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Bacitracin is in a class of medications called antibiotics. Bacitracin works by stopping the growth of bacteria.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • It's a first aid antibiotic you put directly on the skin to help prevent infection in minor cuts, scrapes, and burns. It's not meant for serious or deep wounds — just everyday smal...
  • What exactly is bacitracin topical used for?
  • Use a small amount — about the size of the tip of your finger — and apply it to the clean, dry area 1 to 3 times a day. You can put a sterile bandage over it if you like. Don't use...
  • Not without checking with your doctor first. Bacitracin topical is meant for minor wounds. Deep or puncture wounds, animal bites, and serious burns need a doctor's evaluation — thi...
📖 Read our full Bacitracin Topical guide →
7
Nutrient depletion considerations

Bacitracin may be associated with lower levels of 7 nutrients — worth a chat with your pharmacist, not a cause for alarm.

An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.

🧪 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 statespetrolatum

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 DailyMedingredient 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.

💲 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.
Try another pack size: 9 g 25 packets 144 packets
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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Bacitracin Zinc 500 [USP'U]/g 00536-1263-28 Rugby 1 tube $0.079 Availability likely
Leader Bacitracin Zinc 500 [USP'U]/g 70000-0547-01 Cardinal 1 tube $0.079 Availability likely
Good Neighbor Pharmacy Bacitracin Zinc 500 [iU]/g 24385-0060-03 AmerisourceBergen 1 tube $0.095 Availability likely
Bacitracin Zinc 500 [USP'U]/g 70677-1211-01 STRATEGIC 1 tube $0.095 Availability likely
antibiotic Bacitracin Zinc 500 [iU]/g 49348-0154-72 Strategic 1 tube $0.095 Discontinued
Bacitracin Zinc 500 [USP'U]/g 51672-2075-01 Sun 1 tube $0.187 Availability likely
Bacitracin Zinc 500 [USP'U]/g 68001-0531-45 BluePoint 1 tube $0.187 Availability likely
Bacitracin Zinc 500 [iU]/g 00404-0170-50 Henry 1 tube FDA listed
Bacitracin Zinc 500 [iU]/g 00404-0172-50 Henry 144 packets FDA listed
Major Bacitracin 500 [USP'U]/g 00904-7023-67 Major 144 packets FDA listed
Sheffield Bacitracin Zinc 500 [USP'U]/g 11527-0163-15 Sheffield 1 tube FDA listed
First Aid Antibiotic 500 [USP'U]/g 11673-0396-01 TARGET 1 tube FDA listed
First Aid Antibiotic 500 [USP'U]/g 11673-0790-14 Target 1 tube FDA listed
Bacitracin Zinc 500 [USP'U]/g 21922-0091-04 Encube 1 tube FDA listed
TopCare Bacitracin Zinc 500 [iU]/g 36800-0089-02 Topco 1 tube FDA listed
Medi-First Bacitracin Zinc 500 [USP'U]/g 47682-0863-66 Unifirst 1 tube FDA listed
Bacitracin Zinc 500 [USP'U]/g 49035-0510-26 EQUATE 1 tube FDA listed
Bacitracin Zinc 500 [USP'U]/g 50090-4706-00 A-S 1 tube FDA listed
Live Better Bacitracin Zinc 500 [iU]/g 51143-0075-02 The 1 tube FDA listed
CAREALL Bacitracin 500 [USP'U]/g 51824-0003-01 New 28 g FDA listed
Bacitracin Zinc 500 [USP'U]/g 52000-0059-01 Universal 1 tube Discontinued
Medpride First Aid 500 [USP'U]/g 52410-3035-02 Shield 9 g FDA listed
First Aid Antibiotic 500 [USP'U]/g 53329-0089-01 Medline 1 tube FDA listed
ProCure Bacitracin Zinc 500 [iU]/g 55681-0016-01 Twin 28.3 g FDA listed
procureFirst Aid Antibio First Aid Antibiotic 500 U/g 55681-0218-01 TWIN 9 g FDA listed
Bacitracin Zinc 500 [USP'U]/g 57896-0145-14 Geri-Care 144 packets FDA listed
Bacitracin Zinc 500 [USP'U]/g 58980-0011-01 STRATUS 144 packets FDA listed
Bacitracin 500 [iU]/gthis 59898-0720-01 Water-Jel 1728 packets FDA listed
Single Antibiotic 500 [iU]/g 61010-4404-01 Safetec 28.4 g FDA listed
Family Care First Aid 500 [USP'U]/g 65923-0491-33 United 1 tube FDA listed
Winco Bacitracin Zinc 500 [USP'U]/g 67091-0270-28 WinCo 1 tube FDA listed
Bacitracin Zinc 500 [USP'U]/g 67777-0008-10 Dynarex 144 packets FDA listed
Premier Value Bacitracin Zinc 500 [USP'U]/g 68016-0107-01 Pharmacy 1 tube FDA listed
Sion Biotext Bacitracin Zinc 500 [iU]/g 68786-0500-01 Sion 28 g FDA listed
Bacitracin 500 [USP'U]/g 69396-0027-01 Trifecta 1 tube FDA listed
Bacitracin Zinc 500 [USP'U]/g 69396-0098-09 Trifecta 144 packets FDA listed
Bacitracin Zinc 500 [USP'U]/g 69396-0104-09 Trifecta 144 packets FDA listed
Always Save Bacitracin Zinc 500 [USP'U]/g 69396-0148-01 Trifecta 1 tube FDA listed
Bacitracin Zinc 500 [USP'U]/g 69396-0163-09 Trifecta 144 packets FDA listed
FifthPulse Bacitracin Zinc 4oz 500 [iU]/g 69571-0012-02 Front 113.4 g FDA listed
FifthPulse Bacitracin Zinc 1oz 500 [iU]/g 69571-0013-01 Front 28.4 g FDA listed
Gerigentle-Bacitracin zinc 500 [USP'U]/g 69771-0106-34 Geri-Gentle 144 packets FDA listed
Vitastem ULTRA 500 U/mL 71262-0007-15 ViaDerma 1 bottle FDA listed
Equate 500 [USP'U]/g 79903-0372-01 Walmart 1 tube FDA listed
Drs. Antibiotic Bacitracin 500 [USP'U]/g 80489-0006-01 OL 1 tube FDA listed
Bacitracin Zinc 500 [USP'U]/g 83324-0040-01 Chain 1 tube FDA listed
ElixirBaciShield First Aid 500 [USP'U]/g 84546-0002-01 ELIXIR 28.3 g FDA listed
Bacitracin Zinc 500 [USP'U]/g 87236-0001-01 Aldermed 1 tube FDA listed
FifthPulse Bacitracin Zinc 500 U/g 87525-0001-01 WeCare 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

🏛️
2010
On the market since
Nov 2010
📍
2026
Currently FDA-listed
16 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.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Bacitracin — the program that covers self-administered drugs. 1 manufacturer.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Bacitracin. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$3.9K
Claims incl. refills
44
Beneficiaries
42
Spend / beneficiary
$92.36
Spend / claim
$88.16
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Bacitracin — the ingredient across all brands.

Top reported reactions

Drug Hypersensitivity398
Pain238
Nausea236
Dyspnoea222
Diarrhoea218
Fatigue206
Rash206

Reporter sex

4,414 reports
Male · 38%
Female · 62%
Unknown · 0%

Serious outcomes

Death360
Disabling107
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 352 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
59898-0720-01 You're viewing this 1728 PACKET in 1 CARTON (59898-720-01) / .9 g in 1 PACKET 2010-11-07 Active
59898-0720-02 144 PACKET in 1 BOX, UNIT-DOSE (59898-720-02) / .9 g in 1 PACKET 2010-11-07 Active
59898-0720-03 25 PACKET in 1 BOX, UNIT-DOSE (59898-720-03) / .9 g in 1 PACKET 2010-11-07 Active
59898-0720-36 .9 g in 1 PACKET (59898-720-36) 2010-11-07 Active

Pack size FAQ

What quantity is in NDC 59898-0720-01?
NDC 59898-0720-01 contains 1728 packets — 1728 packet in 1 carton / .9 g in 1 packet.
What is the difference between NDC 59898-0720-01 and NDC 59898-0720-36?
Both are Bacitracin 500 [iU]/g Ointment — the drug itself is identical. NDC 59898-0720-01 is the 1728 packets package, while NDC 59898-0720-36 is the 9 g package.
What NDC number is used to bill for this package of Bacitracin 500 [iU]/g Ointment?
Bill NDC 59898-0720-01 — the 11-digit billing format is 59898072001. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 59898-720-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 59898-0720-01, written without dashes as 59898072001. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 59898-0720-01, the first segment (59898) is the labeler code FDA assigned to Water-Jel Technologies; the middle segment (0720) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Water-Jel Technologies. 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 3 other package presentations of this same product, including 9 g (59898-0720-36), 25 packets (59898-0720-03), 144 packets (59898-0720-02). 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?
Water-Jel Technologies 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.

📄 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 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 the 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 94 words

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

🧪 Active Ingredient 6 words

Active ingredient Bacitracin zinc 500 units

🧪 Inactive Ingredients 3 words

Inactive ingredient petrolatum

🎯 Purpose 4 words

Purpose First aid antibiotic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
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.