ear drops Carbamide Peroxide 6.5% .065 mg/mL Liquid
by Bionpharma Inc. · 2 BOTTLE, DROPPER in 1 CARTON (69452-377-95) / 15 mL in 1 BOTTLE, DROPPER
NDC 69452-0377-95
🏷️ FDA NDC (as labeled)
69452-377-95
billing pads the product segment with a zero
This package
Contains15 mL in 1 bottle, dropper
Pack sizes2 compare ↓
Also comes in:
15 mL 69452-0377-75
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)
69452-377-95
Product NDC
69452-377
11-digit billing NDC
69452037795
RxCUI
702050
UNII
31PZ2VAU81
Application #
M014
SPL Set ID
e8bcf92c-ad32-49d5-e053-2995a90ae0c6
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2022-09-15
Route
AURICULAR (OTIC)
Dosage form
LIQUID
Substance
CARBAMIDE PEROXIDE
Why two NDCs?
The FDA registers this code as 69452-377-95 — 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 → 69452-0377-95. 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.
🏭 Manufacturer & labeler
LabelerBionpharma Inc.
FDA applicationM014 (OTC MONOGRAPH DRUG)
Labeler code69452
First marketedSep 2022
Product typeHuman Otc Drug
Portfolio163 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
🧪 What is this product?
This is an over-the-counter ear drop liquid containing carbamide peroxide, an oxidizing agent that is typically used to help soften and break up earwax buildup in the ear canal. The product is applied directly into the ear and functions as a ceruminolytic, meaning it works to dissolve or loosen impacted cerumen so it can be more easily removed. Carbamide peroxide ear drops are commonly used for temporary relief of minor ear discomfort related to excess earwax.
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.
💬 Questions about Carbamide Peroxide 6.5%?
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.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.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 mL | 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:
15 mL
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 |
|---|---|---|---|---|---|---|
| Ear Drops Major 6.5 g/100mL 00904-6627-35 | Major | 1 bottle | $0.162 | — | Availability likely | — |
| Major Earwax Removal Drops Earwax Removal Aid 65 mg/mL 00904-7478-35 | Major | 1 bottle | $0.162 | — | Availability likely | — |
| Ear Wax Removal Drops 65 mg/mL 11527-0143-51 | Sheffield | 1 bottle | $0.162 | — | Availability likely | — |
| Good Neighbor Pharmacy Earwax Removal 46122-0556-05 | Amerisource | 1 kit | $0.162 | — | Availability likely | — |
| Good Neighbor Pharmacy Earwax Removal Drops 65 mg/mL 46122-0557-05 | Amerisource | 1 bottle | $0.162 | — | Availability likely | — |
| Leader Earwax Removal Drops Earwax Removal Aid 65 mg/mL 70000-0688-01 | Cardinal | 1 bottle | $0.162 | — | Availability likely | — |
| Foster and Thrive Earwax Removal Kit Ear wax drops 70677-1153-01 | Mckesson | 1 kit | $0.162 | — | Availability likely | — |
| Foster and Thrive Earwax Removal Drops 65 mg/mL 70677-1154-01 | Mckesson | 1 bottle | $0.162 | — | Availability likely | — |
| Deluxe Ear Wash system 00363-2231-10 | Walgreens | 1 kit | — | — | FDA listed | — |
| Ear Wax Removal Drops Up and Up 65 mg/mL 11673-0761-05 | Target | 1 bottle | — | — | FDA listed | — |
| Ear Wax Removal Aid Drops .065 mg/mL 11673-0793-15 | Target | 1 bottle | — | — | FDA listed | — |
| EarWax Removal Kit Rite Aid 11822-1222-07 | Rite | 1 kit | — | — | FDA listed | — |
| EAR WAX RMVL Rite Aid 6.5 g/100mL 11822-1224-01 | Rite | 15 ml | — | — | FDA listed | — |
| Rite Aid Earwax Removal Drops 6.5 g/100mL 11822-6117-00 | Rite | 1 bottle | — | — | FDA listed | — |
| ClearCanal Ear Wax Softerner Drops 65 mg/mL 13709-0230-01 | NeilMed | 1 bottle | — | — | FDA listed | — |
| SuavEar Earwax Removal Aid 65 mg/mL 13709-0312-01 | NEILMED | 1 bottle | — | — | FDA listed | — |
| Wax Out Plus 65 mg/mL 13709-0313-01 | NEILMED | 1 bottle | — | — | FDA listed | — |
| NeilMed Clear Canal Earwax Removal kit 65 mg/mL 13709-0314-01 | NEILMED | 1 bottle | — | — | FDA listed | — |
| Otix Ear wax Removal Drops 65 mg/mL 15579-0838-34 | Bell | 1 bottle | — | — | FDA listed | — |
| Otix Ear wax Removal System Ear wax and Bulb 15579-0839-33 | Bell | 1 kit | — | — | FDA listed | — |
| Ear Wax Removal Aid Drops 65 mg/mL 21130-0793-15 | BETTER | 1 bottle | — | — | FDA listed | — |
| TopCare Earwax Removal Kit 65 mg/mL 36800-0835-33 | TOPCO | 1 bottle | — | — | FDA listed | — |
| Equaline Earwax Removal Drops 65 mg/mL 41163-0835-34 | United | 1 bottle | — | — | FDA listed | — |
| Meijer Earwax Removal Drops 65 mg/mL 41250-0282-34 | Meijer | 1 bottle | — | — | FDA listed | — |
| Meijer Earwax Removal Kit 65 mg/mL 41250-0835-33 | Meijer | 1 bottle | — | — | FDA listed | — |
| Ear Wax Removal Drops Equate 65 mg/mL 49035-0862-01 | WALMART | 1 bottle | — | — | FDA listed | — |
| Debrox 65 mg/mL 50090-4201-00 | A-S | 1 bottle | — | — | FDA listed | — |
| Ear Drops Major 6.5 g/100mL 50090-5273-00 | A-S | 1 bottle | — | — | FDA listed | — |
| Clearcanal Ear Wax Softerner Drops 65 mg/mL 50090-7426-00 | A-S | 1 bottle | — | — | FDA listed | — |
| Foster And Thrive Earwax Removal Drops 65 mg/mL 50090-7510-00 | A-S | 1 bottle | — | — | FDA listed | — |
| GoodSense Ear Wax Removal Kit 6.5 g/100mL 50804-0117-01 | Geiss, | 1 bottle | — | — | FDA listed | — |
| CVS Health Earwax Removal Drops Earwax Removal Aid 65 mg/mL 51316-0822-00 | CVS | 1 bottle | — | — | FDA listed | — |
| CVS Health Earwax Removal Kit 51316-0823-00 | CVS | 1 kit | — | — | FDA listed | — |
| ERO Ear Wax Removal Kit 6.5 g/100mL 52412-0175-01 | Randob | 1 bottle | — | — | FDA listed | — |
| DISCOUNT drug mart FOOD FAIR earwax removal kit 65 mg/mL 53943-0835-33 | Discount | 1 bottle | — | — | FDA listed | — |
| Discount Drug Mart Earwax Removal Drops 65 mg/mL 53943-0838-34 | Discount | 1 bottle | — | — | FDA listed | — |
| Family Wellness Earwax Removal Earwax and Bulb 55319-0835-01 | Family | 1 kit | — | — | FDA listed | — |
| DoloEar 6.5 g/100mL 55758-0506-01 | Pharmadel | 1 bottle | — | — | FDA listed | — |
| Ear Wax Removal Drops 65 mg/mL 57896-0339-05 | GeriCare | 1 bottle | — | — | FDA listed | — |
| Audiologists Choice Earwax Removal System 65 mg/mL 59256-0001-02 | Oaktree | 1 bottle | — | — | FDA listed | — |
| Audiologists Choice Earwax Removal Aid Drops 65 mg/mL 59256-0836-34 | Oaktree | 1 bottle | — | — | FDA listed | — |
| Debrox 65 mg/mL 63029-0321-01 | Medtech | 1 bottle | — | — | FDA listed | — |
| Quality Choice Earwax Removal Kit 65 mg/mL 63868-0026-15 | Chain | 1 bottle | — | — | FDA listed | — |
| Quality Choice Earwax Removal Drops 65 mg/mL 63868-0027-16 | Chain | 1 bottle | — | — | FDA listed | — |
| Best Choice Earwax Removal Kit 65 mg/mL 63941-0835-33 | Valu | 1 bottle | — | — | FDA listed | — |
| Best Choice Earwax Removal Drops 65 mg/mL 63941-0836-34 | Valu | 1 bottle | — | — | FDA listed | — |
| Family Care Earwax Removal .065 mg/mL 65923-0639-15 | United | 1 bottle | — | — | FDA listed | — |
| Wax Away Earwax Removal Aid 65 mg/mL 66354-0005-81 | McKeon | 1 bottle | — | — | FDA listed | — |
| Wax Away Earwax Removal System 65 mg/mL 66354-0006-80 | McKeon | 1 bottle | — | — | FDA listed | — |
| ProRinse Earwax Removal System 65 mg/mL 66354-0007-82 | McKeon | 1 bottle | — | — | FDA listed | — |
| Ear Wax Removal Aid Drops .065 mg/mL 68016-0793-15 | PHARMACY | 1 bottle | — | — | FDA listed | — |
| ENT Essentials Ear Wax Remvoer .065 g/g 68093-4503-01 | Wisconsin | 1 bottle | — | — | FDA listed | — |
| Clinere Ear Wax Remover .065 g/mL 68229-0102-02 | Quest | 1 bottle | — | — | FDA listed | — |
| Good Neighbor Pharmacy Earwax Removal Drops 65 mg/mL 68788-8586-01 | Preferred | 1 bottle | — | — | FDA listed | — |
| GoodSense Ear Wax Removal Kit 6.5 g/100mL 68788-8615-01 | Preferred | 1 bottle | — | — | FDA listed | — |
| Carbamide peroxide 6.5% 65 mg/mL 69168-0488-68 | Allegiant | 1 bottle | — | — | FDA listed | — |
| Harris Teeter Earwax Removal Drops 6.5 g/100mL 69256-0117-01 | Harris | 1 bottle | — | — | FDA listed | — |
| Tech Care Earwax Removal Drops 65 mg/mL 69428-0002-00 | Warner | 1 bottle | — | — | FDA listed | — |
| Tech Care Earwax Removal Kit 69428-0003-00 | Warner | 1 kit | — | — | FDA listed | — |
| ear drops .065 mg/mLthis 69452-0377-95 | Bionpharma | 2 bottles | — | — | FDA listed | — |
| Healthy Ears 6.5 mg/mL 69469-0650-05 | Vitamex | 14.7 ml | — | — | FDA listed | — |
| Ear Drops .065 mg/mL 69842-0097-45 | CVS | 1 bottle | — | — | FDA listed | — |
| Ear Wash Refill CVS 69842-0877-14 | CVS | 1 kit | — | — | FDA listed | — |
| Leader Earwax Removal Kit Earwax Removal Aid and Bulb 70000-0689-01 | Cardinal | 1 kit | — | — | FDA listed | — |
| Good Neighbor Pharmacy Earwax Removal Drops 65 mg/mL 71205-0260-15 | Proficient | 1 bottle | — | — | FDA listed | — |
| CareOne Earwax Removal Drops 65 mg/mL 72476-0838-34 | Retail | 1 bottle | — | — | FDA listed | — |
| WaxRx Ear Wax Removal Aid Drops 6.5 g/100mL 72724-0001-15 | DOCTOR | 15 ml | — | — | FDA listed | — |
| DG Health Earwax Removal kit 65 mg/mL 75712-0301-14 | DOLLAR | 1 bottle | — | — | FDA listed | — |
| TopCare Earwax Removal Drops 65 mg/mL 76162-0836-34 | Topco | 1 bottle | — | — | FDA listed | — |
| Ear Wash Refill Equate 79903-0403-50 | Walmart | 1 kit | — | — | FDA listed | — |
| Wax B Gone Ear Wax Removal Drops 65 mg/mL 82498-0149-15 | SIGMAR, | 1 bottle | — | — | FDA listed | — |
| Freskaro Earwax Removal Aid 6.5 g/100mL 82645-0097-45 | Pharma | 1 bottle | — | — | FDA listed | — |
| Quality Choice Earwax Removal Kit Earwax Removal Aid and Bulb 83324-0282-05 | Chain | 1 kit | — | — | FDA listed | — |
| Quality Choice Earwax Removal Drops Earwax Removal Aid 65 mg/mL 83324-0283-05 | Chain | 1 bottle | — | — | FDA listed | — |
| Lucid Hearing Earwax Removal Kit and Bulb 84320-0001-00 | Hearing | 1 kit | — | — | FDA listed | — |
| Earwax Removal Drops .065 mg/mL 00395-9133-45 | Humco | 1 bottle | — | — | FDA listed | — |
| Earwax Removal Drops .065 mg/mL 52412-0600-05 | Randob | 1 bottle | — | — | FDA listed | — |
| Earwax Removal Drops .065 mg/mL 82645-0910-45 | Pharma | 1 bottle | — | — | FDA listed | — |
| Walgreens Ear Wax Remover .065 mg/mL 00363-2068-15 | Walgreens | 1 bottle | — | — | 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
🏛️
2022
On the market since
Sep 2022
📍
2026
Currently FDA-listed
4 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 69452-0377-95 You're viewing this | 2 BOTTLE, DROPPER in 1 CARTON (69452-377-95) / 15 mL in 1 BOTTLE, DROPPER | 2022-09-15 | Active |
| 69452-0377-75 | 1 BOTTLE, DROPPER in 1 CARTON (69452-377-75) / 15 mL in 1 BOTTLE, DROPPER | 2022-09-15 | Active |
Pack size FAQ
What quantity is in NDC 69452-0377-95?
NDC 69452-0377-95 is listed by the FDA — 2 bottle, dropper in 1 carton / 15 ml in 1 bottle, dropper.
What NDC number is used to bill for this package of ear drops Carbamide Peroxide 6.5% .065 mg/mL Liquid?
Bill NDC 69452-0377-95 — the 11-digit billing format is 69452037795. 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) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 69452-377-95, 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: 69452-0377-95, written without dashes as 69452037795. 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 69452-0377-95, the first segment (69452) is the labeler code FDA assigned to Bionpharma Inc.; the middle segment (0377) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (95) 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 Bionpharma Inc.. 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 bottle (69452-0377-75). 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?
Bionpharma Inc. 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
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses For occasional use as an aid to soften, loosen and remove excessive earwax
⏱️ Dosage and Administration ▾
Directions FOR USE IN THE EAR ONLY Remove any earing aids before use Adults and children over 12 yrs of age: tilt head to the side and place 10 drops into the ear. Tip of applicator should not enter into the ear canal Keep drops in ear for several minutes by keeping head tilted sideways or placing cotton in the ear. Use twice daily for up to 4 days if needed, or as directed by a doctor.
Any wax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe. Children under 12 yrs of age: Consult a physician.
⚠️ Warnings ▾
Warnings Do not use if you have ear drainage or discharge, ear pain, irritation, or rash in the ear or are dizzy; consult a doctor If you have an injury or perforation (hole) of the ear or after ear surgery, unless directed by a doctor for more than 4 consecutive days. If excessive earwax remains after use of this product, consult a doctor. When using this product avoid contact with eyes Stop use and ask a doctor you need to use for more than four days excessive earwax remains after a four day treatment with this product Keep out of the reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredients Carbamide Peroxide 6.5% non USP* *pH differs from USP specifications
🧪 Inactive Ingredients ▾
Inactive ingredients Citric Acid, Flavor, Glycerin, Propylene Glycol, Sodium Lauroyl Sarcosinate, Sodium Stannate, Purified Water.
🎯 Purpose ▾
Purposes Earwax removal aid
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.