![Neosporin Pain Itch Scar Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride 500 [iU]/g; 3.5 mg/g; 10000 [iU]/g; 10 mg/g Ointment, 1 tube — NDC 69968-0093-01 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=55392c48-b5d8-44cd-8c10-6d8668349848&name=Neosporin_3.jpg)
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Neosporin Pain Itch Scar Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride 500 [iU]/g; 3.5 mg/g; 10000 [iU]/g; 10 mg/g Ointment, 1 tube — NDC 69968-0093-1 (Billing 69968-0093-01)
by Kenvue Brands LLC · 1 TUBE in 1 CARTON / 28.3 g in 1 TUBE
This is a package of 1 tube of Neosporin Pain Itch Scar Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride 500 [iU]/g; 3.5 mg/g; 10000 [iU]/g; 10 mg/g Ointment from Kenvue Brands LLC, marketed since Jan 2016 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.
NDC 69968-0093-01
🏷️ FDA NDC (as labeled)
69968-0093-1
billing pads the package segment with a zero
This package
Contains1 tube
Pack sizes2 compare ↓
Main listing for product 69968-0093 · Also comes in:
14.2 g 69968-0093-2
🗂️ 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 →
NDC database record
One package, one record: these facts belong to NDC 69968-0093-1 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 69968 labeler · 0093 product · 1 package
- Package marketed since
- Jan 15, 2016
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC)
- 0312547238090
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
69968-0093-1
Product NDC
69968-0093
11-digit billing NDC
69968009301
NCPDP billing unit
GM — per gram (weight)
RxCUI
1359350
UNII
89Y4M234ES, 057Y626693, 19371312D4, 88AYB867L5
UPC
0312547238090
Application #
M004
SPL Set ID
55392c48-b5d8-44cd-8c10-6d8668349848
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
2016-01-15
Route
TOPICAL
Dosage form
OINTMENT
Substance
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
GCN Seq No
047690
GCN
12623
HICL code
035595
Ingredient (HICL)
Neomycn/Bacitrc/Polymyx/Pramox
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
08:12.02.00
AHFS class
Aminoglycoside Antibiotics
FDB label name
NEOSPORIN-PAIN ITCH SCAR OINT
FDB brand name
Neosporin-Pain Itch Scar
Legend status
O — Over-the-counter (OTC) drug or device
Quick answers
- GSN (GCN sequence number): 047690
- GCN: 12623
- HICL (First Databank): 035595
- AHFS class code: 08:12.02.00
- RxCUI (RxNorm): 1359350
Why two NDCs?
The FDA registers this code as 69968-0093-1 — 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 → 69968-0093-01. 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
Label name NEOSPORIN-PAIN ITCH SCAR OINT Ingredient Neomycn/Bacitrc/Polymyx/Pramox
📖 About the active ingredient MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.
Neomycin, polymyxin, and bacitracin combination is used to prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Neomycin, polymyxin, and bacitracin are in a class of medications called antibiotics. Neomycin, polymyxin, and bacitracin combination works by stopping the growth of bacteria.
Read the full MedlinePlus article ↗🧪 What is this product?
Neosporin Pain Itch Scar is an over-the-counter topical ointment containing three antibiotic ingredients (bacitracin zinc, neomycin sulfate, and polymyxin B sulfate) that are typically used to help prevent bacterial infection in minor cuts, scrapes, and wounds. The ointment also contains pramoxine hydrochloride, a topical anesthetic commonly used to temporarily relieve minor pain and itching. This is an OTC monograph product, meaning it follows FDA's established guidelines for this category of first-aid antibiotic ointments.
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
💬 Questions about Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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.
Try another pack size:
14.2 g
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 8, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 69968-0093-01 You're viewing this Main listing | 1 TUBE in 1 CARTON / 28.3 g in 1 TUBE | 2016-01-15 | — | Active |
| 69968-0093-02 69968-0093-2 | 1 TUBE in 1 CARTON / 14.2 g in 1 TUBE | 2016-01-15 | — | Active |
Pack size FAQ
What quantity is in this package?
This package contains 1 tube — 1 tube in 1 carton / 28.3 g in 1 tube.
How does this package differ from NDC 69968-0093-02?
Both are Neosporin Pain Itch Scar Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride 500 [iU]/g; 3.5 mg/g; 10000 [iU]/g; 10 mg/g Ointment — the drug itself is identical. This page's package is the 1 tube one, while NDC 69968-0093-02 is the 1 tube package.
What NDC number is used to bill for this package of Neosporin Pain Itch Scar Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride 500 [iU]/g; 3.5 mg/g; 10000 [iU]/g; 10 mg/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
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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2016
On the market since
Jan 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.
- FDA Orange Book · refreshed Oct 3, 2026
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 9E8X80D2L0
A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
-
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 N5CFT140R8
A plant oil derived from cottonseed, used in medicines as a solvent or carrier to help dissolve or suspend active ingredients and improve how the body absorbs them.
-
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 statesPetrolatum, Gossypium Herbaceum (Cotton) Seed Oil, Olea Europaea (Olive) Fruit Oil, Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate, Sodium Pyruvate
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.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
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
LabelerKenvue Brands LLC
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code69968
First marketedJan 2016
Product typeHuman Otc Drug
Portfolio567 products on file
More NDCs from Kenvue Brands LLC labeler code 69968
- Neutrogena Healthy Skin Anti-Aging Perfector Sunscreen Broad Spectrum SPF 20 Neutral to Tan 40 Octinoxate and Octisalate 70 mg/mL; 30 mg/mL Lotion NDC 69968-0079-1
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- Neutrogena Healthy Skin Anti-Aging Perfector Sunscreen Broad Spectrum SPF 20 Medium to Deep 60 Octinoxate and Octisalate 70 mg/mL; 30 mg/mL Lotion NDC 69968-0081-1
- Mens Rogaine Extra Strength Unscented Minoxidil 50 mg/mL Solution NDC 69968-0089-1
- Womens Rogaine Unscented Minoxidil 20 mg/mL Solution NDC 69968-0090-1
- Neutrogena All in 1 Acne Control Daily Scrub Salicylic Acid 20 mg/mL Liquid NDC 69968-0092-4
- Neutrogena Beach Defense Water Plus Sun Protection Sunscreen Broad Spectrum SPF30 Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone 30 mg/g; 30 mg/g; 40 mg/g; 20 mg/g; 50 mg/g Spray NDC 69968-0101-6
- Clean and Clear Advantage Acne Spot Treatment Salicylic Acid 20 mg/mL Lotion NDC 69968-0126-1
- Neutrogena Oil Free Acne Wash Cleanser Salicylic Acid 20 mg/mL Cream NDC 69968-0155-6
- Neutrogena On-the-Spot Acne Treatment Vanishing Formula Benzoyl Peroxide 25 mg/g Cream NDC 69968-0164-1
- Neutrogena Beach Defense Water Plus Sun Protection Sunscreen Broad Spectrum SPF70 Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone 50 mg/g; 40 mg/g; 60 mg/g; 30 mg/g; 150 mg/g Aerosol, Spray NDC 69968-0169-6
- Neutrogena Ultra Sheer Body Mist Sunscreen Broad Spectrum SPF 70 Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone 30 mg/g; 150 mg/g; 50 mg/g; 40 mg/g; 60 mg/g Aerosol, Spray NDC 69968-0171-5
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 openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
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 ▾
Uses first aid to help prevent infection and for temporary relief of pain or discomfort in minor: cuts scrapes burns
⏱️ Dosage and Administration ▾
Directions adults and children 2 years of age and older: 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 children under 2 years of age: ask a doctor
⚠️ Warnings ▾
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 symptoms persist for more than 1 week, or clear up and occur again within a few days 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 ▾
Other information store at 20° to 25°C (68° to 77°F)
🧪 Active Ingredient ▾
Active ingredients (in each gram) Purpose Bacitracin 500 units First aid antibiotic Neomycin 3.5 mg First aid antibiotic Polymyxin B 10,000 units First aid antibiotic Pramoxine HCl 10 mg External analgesic
🧪 Inactive Ingredients ▾
Inactive ingredients Petrolatum, Gossypium Herbaceum (Cotton) Seed Oil, Olea Europaea (Olive) Fruit Oil, Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate, Sodium Pyruvate
🎯 Purpose ▾
Active ingredients (in each gram) Purpose Bacitracin 500 units First aid antibiotic Neomycin 3.5 mg First aid antibiotic Polymyxin B 10,000 units First aid antibiotic Pramoxine HCl 10 mg External analgesic
📄 Do Not Use ▾
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 ▾
Ask a doctor before use if you have deep or puncture wounds animal bites serious burns
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if you need to use longer than 1 week condition persists or gets worse symptoms persist for more than 1 week, or clear up and occur again within a few days rash or other allergic reaction develops
📄 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.
📄 Questions or Comments ▾
Questions? call toll-free 800-223-0182 or 215-273-8755 (collect)
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL - 28.3 g Tube Carton #1 DOCTOR RECOMMENDED BRAND NEOSPORIN ® + PAIN + ITCH + SCAR Maximum Strength: Infection Protection, Pain and Itch Relief 24-Hour Infection Protection Minimizes the Appearance of Scars NO STING OINTMENT FIRST AID ANTIBIOTIC/PAIN RELIEVING OINTMENT Bacitracin Zinc - Neomycin Sulfate - Polymyxin B Sulfate – Pramoxine HCl NET WT
1.0OZ (28.3 g) Neosporin
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 ↗
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 Neosporin Pain Itch Scar (this brand).
Top reported reactions
Age at onset
Reporter sex
Female · 100%
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 Kenvue Brands LLC. 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 1 other package presentation of this same product, including 1 tube (69968-0093-02). 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?
Kenvue Brands 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.
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.