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Bacitracin Zinc First Aid Antibiotic 500 [USP'U]/g Ointment — NDC 67777-0008-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Bacitracin Zinc First Aid Antibiotic 500 [USP'U]/g Ointment — NDC 67777-008-10 (Billing 67777-0008-10)

by Dynarex Corporation · 1728 BOX in 1 CASE / 144 PACKET in 1 BOX / .9 g in 1 PACKET

This is a package of Bacitracin Zinc First Aid Antibiotic 500 [USP'U]/g Ointment from Dynarex Corporation, marketed since Feb 2018 and currently FDA-listed. It is the main listing for this product, which comes in 5 package sizes.

NDC 67777-0008-10
🏷️ FDA NDC (as labeled) 67777-008-10 billing pads the product segment with a zero
This package
Contains.9 g in 1 packet Pack sizes5 compare ↓
Main listing for product 67777-008 · Also comes in: 14.2 g 67777-008-20 28.4 g 67777-008-30 113 g 67777-008-50 12 jars 67777-008-60
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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

NDC database record

One package, one record: these facts belong to NDC 67777-008-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
67777 labeler · 008 product · 10 package
Package marketed since
Feb 16, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0616784117225, 0616784117126, 0616784117317, 0616784117522 +1 more
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 67777-008-10
Product NDC 67777-008
11-digit billing NDC 67777000810
NCPDP billing unit EA — each (per item)
RxCUI 1366116
UNII 89Y4M234ES
UPC 0616784117225, 0616784117126, 0616784117317, 0616784117522 +1 more
Application # M004
SPL Set ID 82cf8dd0-eef6-5871-e053-2991aa0a38cf
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 2018-02-16
Route TOPICAL
Dosage form OINTMENT
Substance BACITRACIN ZINC

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 90100010104210
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
Quick answers
  • GSN (GCN sequence number): 030028
  • GCN: 31813
  • GPI-14 (Medi-Span): 90100010104210
  • HICL (First Databank): 006091
  • AHFS class code: 84:04.04.00
  • RxCUI (RxNorm): 1366116
Why two NDCs? The FDA registers this code as 67777-008-10 — 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 → 67777-0008-10. 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

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 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 →

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.
Try another pack size: 14.2 g 28.4 g 113 g 12 jars
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
67777-0008-10 You're viewing this Main listing 1728 BOX in 1 CASE / 144 PACKET in 1 BOX / .9 g in 1 PACKET 2018-02-16 — Active
67777-0008-20 67777-008-20 72 BOX in 1 CASE / 1 TUBE in 1 BOX / 14.2 g in 1 TUBE 2018-02-16 — Active
67777-0008-30 67777-008-30 72 BOX in 1 CASE / 1 TUBE in 1 BOX / 28.4 g in 1 TUBE 2018-02-16 — Active
67777-0008-50 67777-008-50 72 BOX in 1 CASE / 1 TUBE in 1 BOX / 113 g in 1 TUBE 2018-02-16 — Active
67777-0008-60 67777-008-60 12 JAR in 1 CASE / 425 g in 1 JAR 2018-02-16 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1728 box in 1 case / 144 packet in 1 box / .9 g in 1 packet.
What NDC number is used to bill for this package of Bacitracin Zinc First Aid Antibiotic 500 [USP'U]/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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Bacitracin Zinc 500 [USP'U]/g 00536-1263-28 Rugby 1 tube $0.074 — Availability likely —
Leader Bacitracin Zinc 500 [USP'U]/g 70000-0547-01 Cardinal 1 tube $0.074 — Availability likely —
Good Neighbor Pharmacy Bacitracin Zinc 500 [iU]/g 24385-0060-03 AmerisourceBergen 1 tube $0.093 — Availability likely —
Bacitracin Zinc 500 [USP'U]/g 70677-1211-01 STRATEGIC 1 tube $0.093 — 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 $0.186 — Availability likely —
Bacitracin Zinc 500 [USP'U]/g 68001-0531-45 BluePoint 1 tube $0.186 — 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 — — Discontinued —
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]/g 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]/gthis 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 —
TheraCare Bacitracin Zinc 500 [USP'U]/g 71101-0019-01 Veridian 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

🏛️
2018
On the market since
Feb 2018
📍
2026
Currently FDA-listed
8 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.

🧪 Avoiding an ingredient? See Bacitracin Topical inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 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.

Manufacturer & labeler

LabelerDynarex Corporation
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code67777
First marketedFeb 2018
Product typeHuman Otc Drug
Portfolio60 products on file

More NDCs from Dynarex Corporation labeler code 67777

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Uses First aid to help prevent infection in minor cuts, scrapes, and 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 89 words ▾

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 Stop use and ask a doctor if the condition persists or gets worse, or if a rash or other allergic reaction develops If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 24 words ▾

Other Information Store at room temperature Avoid excessive heat and humidity Tamper Evident. Do not use if inner seal is torn, cut or opened.

🧪 Active Ingredient 9 words ▾

Active Ingredient Bacitracin Zinc (500 units in each gram)

🧪 Inactive Ingredients 9 words ▾

Inactive Ingredients Hard Paraffin, Liquid Paraffin, White Soft Paraffin

🎯 Purpose 4 words ▾

Purpose First Aid Antibiotic

📄 Do Not Use 32 words ▾

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 17 words ▾

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

📄 Stop Use and Ask a Doctor If 22 words ▾

Stop use and ask a doctor if the condition persists or gets worse, or if a rash or other allergic reaction develops

📄 Keep Out of Reach of Children 13 words ▾

If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 37 words ▾

1172 Label 1172 Bacitracin Zinc 1172 BX MASTER

1173 Label 1173 Bacitracin Zinc 1173 BX MASTER

1175 Label 1175 Bacitracin Zinc 1175 BX MASTER

1176 Label 1176 IN MASTER

1171 Label 1171 Bacitracin Zinc 1171 BX GVIN010

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

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 Zinc (this brand).

Top reported reactions

Drug Hypersensitivity27
Dyspnoea9
Nausea9
Diarrhoea8
Fatigue8
Abdominal Pain7
Blood Glucose Increased7

Age at onset

Child3
Adolescent1
Adult10
Elderly6

Reporter sex

166 reports
Male · 46%
Female · 53%
Unknown · 1%
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 15 3
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.

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 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 4 other package presentations of this same product, including 1 tube (67777-0008-20), 1 tube (67777-0008-30), 1 tube (67777-0008-50). 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.
← 67777-0007-50 · Dynarex 67777-0009-40 · Dynarex →
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.