HomeNDC LookupIngredientsCarbamide Peroxide › 41250-0282-34
Meijer Earwax Removal Drops CARBAMIDE PEROXIDE 65 mg/mL Solution/ Drops — NDC 41250-0282-34 package photo

Meijer Earwax Removal Drops CARBAMIDE PEROXIDE 65 mg/mL Solution/ Drops

by Meijer Distribution Inc · 1 BOTTLE in 1 BOX (41250-282-34) / 15 mL in 1 BOTTLE
NDC 41250-0282-34
🏷️ FDA NDC (as labeled) 41250-282-34 billing pads the product segment with a zero
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 →
⚠️
Other active recalls for Carbamide Peroxide (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jun 25, 2026 — SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). (Bell Pharmaceuticals, Inc) · FDA recall D-0680-2026
Class II · Jun 25, 2026 — SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). (Bell Pharmaceuticals, Inc) · FDA recall D-0679-2026
Class II · Jun 25, 2026 — SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). (Bell Pharmaceuticals, Inc) · FDA recall D-0685-2026
Class II · Jun 25, 2026 — SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). (Bell Pharmaceuticals, Inc) · FDA recall D-0683-2026
Class II · Jun 25, 2026 — SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). (Bell Pharmaceuticals, Inc) · FDA recall D-0688-2026
Class II · Jun 25, 2026 — SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). (Bell Pharmaceuticals, Inc) · FDA recall D-0687-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 41250-282-34
Product NDC 41250-282
11-digit billing NDC 41250028234
RxCUI 702050
UNII 31PZ2VAU81
UPC 0713733296519
Application # M014
SPL Set ID 900108c6-0324-644a-e053-2a95a90a3b2b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-11-27
Route AURICULAR (OTIC)
Dosage form SOLUTION/ DROPS
Substance CARBAMIDE PEROXIDE
Why two NDCs? The FDA registers this code as 41250-282-34 — 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 → 41250-0282-34. 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

LabelerMeijer Distribution Inc
FDA applicationM014 (OTC MONOGRAPH DRUG)
Labeler code41250
First marketedNov 2014
Product typeHuman Otc Drug
Portfolio245 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?

Meijer Earwax Removal Drops is an over-the-counter solution applied directly into the ear canal. It contains carbamide peroxide, an ingredient that typically breaks down and helps soften earwax buildup so it can be more easily removed. This product is marketed under FDA's monograph rules for nonprescription earwax removal aids.

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.

🧪 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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesanhydrous citric acid, glycerin, propylene glycol, sodium citrate, sodium lauryl sulfate, water

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 DailyMedingredient 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 systemPer mLPer 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

ProductLabelerPackNADAC/unitTEStatusPrice 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/mLthis 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/mL 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
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

🏛️
2014
On the market since
Nov 2014
📍
2026
Currently FDA-listed
12 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 NDCDescription Marketing startStatus
41250-0282-34 You're viewing this 1 BOTTLE in 1 BOX (41250-282-34) / 15 mL in 1 BOTTLE 2014-11-27 Active

🧭 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 41250-282-34, 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: 41250-0282-34, written without dashes as 41250028234. 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 41250-0282-34, the first segment (41250) is the labeler code FDA assigned to Meijer Distribution Inc; the middle segment (0282) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (34) 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 Meijer Distribution Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Meijer Distribution 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 15 words

Uses for occasional use as an aid to soften, loosen, and remove excessive ear wax

⏱️ Dosage and Administration 98 words

Directions FOR USE IN THE EAR ONLY Adults and children over 12 years of age: Tilt head sideways and place 5 to 10 drops into ear Tip of applicator should not enter ear canal Keep drops in ear for several minutes by keeping head tilted 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 my be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe Children under 12 years: consult a doctor 0

⚠️ Warnings 95 words

Warnings For use in the ear only Ask a doctor before use if you have ear drainage or discharge ear pain irritation, or rash in the ear dizziness an injury or perforation (hole) of the ear drum recently had ear surgery When using this product avoid contact with the eyes Stop use and ask a doctor if you need to use for more than 4 days excessive ear wax remains after use of this product Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center (1-800-222-1222) right away.

🧪 Active Ingredient 10 words

Active ingredient Carbamide peroxide 6.5% Purpose Ear wax removal aid

🧪 Inactive Ingredients 14 words

Inactive ingredients anhydrous citric acid, glycerin, propylene glycol, sodium citrate, sodium lauryl sulfate, water

🎯 Purpose 5 words

Purpose Ear wax removal aid

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.