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BACITRACIN 500 [USP'U]/g Ointment, 28.4 g — NDC 84387-0002-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

BACITRACIN 500 [USP'U]/g Ointment, 28.4 g — NDC 84387-002-01 (Billing 84387-0002-01)

by ALLIED TRADE LINK LLC · 28.4 g in 1 TUBE

This is a package of 28.4 g of BACITRACIN 500 [USP'U]/g Ointment from ALLIED TRADE LINK LLC, marketed since Oct 2024 and currently FDA-listed. It is this product's only package size.

NDC 84387-0002-01
🏷️ FDA NDC (as labeled) 84387-002-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ 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 →

This page is curated, coded, and maintained by

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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84387-002-01
Product NDC 84387-002
11-digit billing NDC 84387000201
RxCUI 1648110
UNII 58H6RWO52I
Application # M004
SPL Set ID 253e5b98-c64f-3226-e063-6294a90a9352
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 2024-10-24
Route TOPICAL
Dosage form OINTMENT
Substance BACITRACIN
Quick answers
  • RxCUI (RxNorm): 1648110
Why two NDCs? The FDA registers this code as 84387-002-01 — 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 → 84387-0002-01. 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 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 is first aid to help prevent infection in minor cuts, scrapes, and burns. One cream product also has directions for athlete's foot, ringworm and jock itch.
  • Clean the area, then put on a small amount, about the size of your fingertip. Do this 1 to 3 times a day, and you can cover it with a sterile bandage. One cream product is used as...
  • Not longer than 1 week unless a doctor tells you to. If the problem is not getting better or gets worse, stop and check with a doctor.
  • Stop if you get a rash or any allergic reaction, and talk to a doctor. Don't use it if you are allergic to any ingredient.
📖 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.

🧪 Full Bacitracin nutrient depletion report →
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.

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
84387-0002-01 You're viewing this Main listing 28.4 g in 1 TUBE 2024-10-24 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Bacitracin 500 U/g 00536-1256-28 RUGBY 30 g $0.055 — Availability likely —
Bacitracin 500 [USP'U]/g 00713-0280-31 Cosette 28.4 g $0.073 — Availability likely —
Bacitracin 500 [iU]/g 68001-0477-46 BluePoint 1 tube $0.094 — Availability likely —
Bacitracin 500 [USP'U]/g 45802-0060-01 Padagis 1 tube $0.117 — Availability likely —
Major Bacitracin 500 [USP'U]/g 00904-7402-67 Major 144 packets $0.121 — FDA listed —
signature care first aid antibiotic 500 [USP'U]/g 21130-0757-64 Safeway 1 tube — — FDA listed —
Bacitracin 500 [USP'U]/g 30142-0536-64 Kroger 1 tube — — FDA listed —
Antibiotic 500 [USP'U]/g 36800-0536-64 Topco 1 tube — — FDA listed —
bacitracin 500 [USP'U]/g 37808-0536-64 H 1 tube — — FDA listed —
MediChoice Bacitracin 500 [iU]/g 39892-0810-01 O&M 144 packets — — FDA listed —
Bacitracin 500 [USP'U]/g 41226-0880-02 Kroger 1 tube — — FDA listed —
Bacitracin 500 [USP'U]/g 41250-0844-64 Meijer 1 tube — — FDA listed —
first aid antibiotic 500 [USP'U]/g 42507-0536-64 HyVee 1 tube — — FDA listed —
Bacitracin 500 [USP'U]/g 50090-0815-00 A-S 1 tube — — FDA listed —
Bacitracin 500 [USP'U]/g 50090-0845-00 A-S 144 packets — — FDA listed —
Rexall Antibiotic 500 [USP'U]/g 55910-0536-64 Dolgencorp, 1 tube — — FDA listed —
Publix Bacitracin Zinc 500 [USP'U]/g 56062-0815-28 PUBLIX 1 tube — — FDA listed —
Bacitracin 500 [USP'U]/g 59779-0536-64 CVS 1 tube — — FDA listed —
Bacitracin 500 [iU]/g 63187-0299-01 Proficient 28.35 g — — FDA listed —
Bacitracin 500 [USP'U]/1000mg 67777-0116-10 Dynarex 144 packets — — FDA listed —
Bacitracin 500 [USP'U]/g 68071-5253-03 NuCare 28.4 g — — FDA listed —
Bacitracin 500 [USP'U]/g 68788-8643-02 Preferred 28.4 g — — FDA listed —
Bacitracin 500 [USP'U]/g 68788-9794-02 Preferred 28 g — — FDA listed —
TheraCare Bacitracin Zinc 500 [USP'U]/g 71101-0019-01 Veridian 1 tube — — FDA listed —
Bacitracin 500 [USP'U]/g 71205-0057-01 Proficient 28.4 g — — FDA listed —
Vitastem Ultra First Aid Antibiotic 500 U/g 71262-0013-15 Viaderma 1 bottle — — FDA listed —
Viaderma Care First Aid 500 U/g 71262-0015-15 ViaDerma 1 bottle — — FDA listed —
Bacitracin 500 [USP'U]/g 71335-2731-01 Bryant 144 packets — — FDA listed —
Bacitracin 500 [USP'U]/g 72162-2280-02 Bryant 144 packets — — FDA listed —
astonea First Aid 500 [USP'U]/g 77338-0303-52 ASTONEA 9 g — — FDA listed —
Bacitracin 500 [USP'U]/gthis 84387-0002-01 ALLIED 28.4 g — — FDA listed —
Bacitracin 500 [iU]/g 87236-0000-01 AlderMed 1 tube — — FDA listed —
Medi-First Bacitracin Zinc 500 [USP'U]/g 47682-0863-66 Unifirst 1 tube — — FDA listed —
Zapotol Bacitracin 500 [USP'U]/g 59428-0135-14 Zapatol 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

🏛️
2024
On the market since
Oct 2024
📍
2026
Currently FDA-listed
2 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 T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII B6E5W8RQJ4
    White petrolatum is a purified mineral oil product used as a lubricant and skin protectant in medications. It helps pills slide through manufacturing equipment and can soften or protect the skin when applied topically.

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

The official label also statesMineral Oil, Paraffin, 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

LabelerALLIED TRADE LINK LLC
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code84387
First marketedOct 2024
Product typeHuman Otc Drug
Portfolio8 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.

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 40 words ▾

DIRECTION 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.

⏱️ Dosage and Administration 98 words ▾

dosage and administration Clean the affected area and dry thoroughly Apply a thin layer of the cream over affected area twice daily (morning and night) or as directed by a doctor Supervise children in the use of this product For athlete's foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily For athlete's foot and ringworm, use daily for 4 weeks For jock itch, use daily for 2 weeks If condition persists longer, consult a doctor This product is not effective on the scalp or nails

⚠️ Warnings 5 words ▾

WARNINGS For External Use Only

🧪 Active Ingredient 15 words ▾

ACTIVE INGRIDIENT Active Ingredient (in each gram) Purpose Bacitracin 500 units ............................................................................................................................................................................................................................................................. First Aid Antibiotic

🧪 Inactive Ingredients 7 words ▾

INACTIVE INGREDIENTS Mineral Oil, Paraffin, White Petrolatum

🎯 Purpose 26 words ▾

Active Ingredient (in each gram) Purpose Bacitracin 500 units ............................................................................................................................................................................................................................................................. First Aid Antibiotic Active Ingredient (in each gram) Purpose Bacitracin 500 units .............................................................................................................................................................................................................................................................

First Aid Antibiotic

📄 Do Not Use 59 words ▾

DO NOT USE 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.

DO NOT USE Stop use and ask a doctor if the condition persists or gets worse, or if a rash or other allergic reaction develops.

📄 Ask a Doctor Before Use If 20 words ▾

ASK A DOCTOR Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns.

📄 When Using This Product 14 words ▾

USES Uses First aid to help prevent infection in minor cuts, scrapes, and burns

📄 Keep Out of Reach of Children 25 words ▾

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

📄 Other Information 51 words ▾

OTHER INFORMATION Do not use if seal on the tube is damaged or is not visible. To open, unscrew cap, pull tab to remove foil seal Store at room temperature See crimp of tube or carton for Lot Number and Expiry Date Preserve in well-closed containers, preferably at controlled room temperature.

📄 Package Label / Principal Display Panel 1 words ▾

BACITRICIN

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

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.

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 ALLIED TRADE LINK LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
ALLIED TRADE LINK LLC 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.
← 84387-0001-01 · ALLIED 84387-0003-01 · ALLIED →
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.