![Bacitracin 500 [USP'U]/1000mg Ointment — NDC 67777-0116-20 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=7f8752c7-6839-261d-e053-2991aa0a0c30&name=1161+BX+MASTER+%28R220112-3%29.jpg)
Bacitracin 500 [USP'U]/1000mg Ointment
by Dynarex Corporation · 72 TUBE in 1 CASE (67777-116-20) / 14000 mg in 1 TUBE (67777-116-21)
NDC 67777-0116-20
🏷️ FDA NDC (as labeled)
67777-116-20
billing pads the product segment with a zero
This package
Contains14000 mg in 1 tube
Pack sizes3 compare ↓
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 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)
67777-116-20
Product NDC
67777-116
11-digit billing NDC
67777011620
NCPDP billing unit
GM — per gram (weight)
RxCUI
1648110
UNII
58H6RWO52I
UPC
0616784116228, 0616784116310, 0616784116129
Application #
M004
SPL Set ID
7f8752c7-6839-261d-e053-2991aa0a0c30
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
2016-09-12
Route
TOPICAL
Dosage form
OINTMENT
Substance
BACITRACIN
GPI-14
90100010004210
GCN Seq No
007731
GCN
31812
HICL code
004047
Ingredient (HICL)
Bacitracin
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 500 UNIT/GM OINTMNT
FDB brand name
Bacitracin
Legend status
O — Over-the-counter (OTC) drug or device
Why two NDCs?
The FDA registers this code as 67777-116-20 — 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 → 67777-0116-20. 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
LabelerDynarex Corporation
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code67777
First marketedSep 2016
Product typeHuman Otc Drug
Portfolio60 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 500 UNIT/GM OINTMNT Ingredient Bacitracin
📖 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...
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Bacitracin — tap one for details:
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.
BIOTIN
Insignificant Depletion
FOLIC ACID
Insignificant Depletion
RIBOFLAVIN
Insignificant Depletion
THIAMINE
Insignificant Depletion
VITAMIN B12
Insignificant Depletion
+2 more
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.
💬 Questions about Bacitracin?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 statesHard Paraffin, Liquid Paraffin, White Soft Paraffin
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.
💲 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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Bacitracin 500 U/g 00536-1256-28 | RUGBY | 30 g | $0.054 | — | Availability likely | — |
| Bacitracin 500 [USP'U]/g 00713-0280-31 | Cosette | 28.4 g | $0.074 | — | 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 | $0.114 | — | 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]/1000mgthis 67777-0116-20 | Dynarex | 72 tubes | — | — | 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]/g 84387-0002-01 | ALLIED | 28.4 g | — | — | FDA listed | — |
| Bacitracin 500 [iU]/g 87236-0000-01 | AlderMed | 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
🏛️
2016
On the market since
Sep 2016
📍
2026
Currently FDA-listed
10 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
Reporter sex
Male · 38%
Female · 62%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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 NDC | Description | Marketing start | Status |
|---|---|---|---|
| 67777-0116-10 | 1728 BOX in 1 CASE (67777-116-10) / 144 PACKET in 1 BOX (67777-116-11) / 900 mg in 1 PACKET | 2016-09-12 | Active |
| 67777-0116-20 You're viewing this | 72 TUBE in 1 CASE (67777-116-20) / 14000 mg in 1 TUBE (67777-116-21) | 2016-09-12 | Active |
| 67777-0116-30 | 72 BOX in 1 CASE (67777-116-30) / 1 TUBE in 1 BOX (67777-116-31) / 28400 mg in 1 TUBE | 2016-09-12 | Active |
Pack size FAQ
What quantity is in NDC 67777-0116-20?
NDC 67777-0116-20 is listed by the FDA — 72 tube in 1 case / 14000 mg in 1 tube.
What NDC number is used to bill for this package of Bacitracin 500 [USP'U]/1000mg Ointment?
Bill NDC 67777-0116-20 — the 11-digit billing format is 67777011620. 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 67777-116-20, 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: 67777-0116-20, written without dashes as 67777011620. 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 67777-0116-20, the first segment (67777) is the labeler code FDA assigned to Dynarex Corporation; the middle segment (0116) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (20) 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 Dynarex 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 1 tube (67777-0116-30), 144 packets (67777-0116-10). 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?
Dynarex 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.
📄 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
🎯 Indications and Usage ▾
Use First aid to help prevent infection in minor cuts, scrapes, and burns
⏱️ Dosage and Administration ▾
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 ▾
Warnings For External Use Only Do not use In the eyes or apply 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 deep or puncture wounds, animal bites, or serious burns If swallowed, get medical help or contact a Poison Control Center right away.
📦 Storage and Handling ▾
Other information Store at room temperature
🧪 Active Ingredient ▾
Active Ingredient Bacitracin (500 units in each gram)
🧪 Inactive Ingredients ▾
Inactive ingredients Hard Paraffin, Liquid Paraffin, White Soft Paraffin
🎯 Purpose ▾
Purpose First Aid Antibiotic
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 ↗
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.