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Hydrogen Peroxide Lil Drug Store Products 3 mL/100mL Liquid, 473 mL — NDC 66715-6846-0 (Billing 66715-6846-00)

by Lil' Drug Store Products, Inc · 473 mL in 1 BOTTLE, PLASTIC

This is a package of 473 mL of Hydrogen Peroxide Lil Drug Store Products 3 mL/100mL Liquid from Lil' Drug Store Products, Inc, marketed since Dec 2014 and currently FDA-listed. It is this product's only package size.

NDC 66715-6846-00
🏷️ FDA NDC (as labeled) 66715-6846-0 billing pads the package segment with a zero
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 66715-6846-0 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
66715 labeler · 6846 product · 0 package
Package marketed since
Aug 15, 2016
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0366715684608
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 66715-6846-0
Product NDC 66715-6846
11-digit billing NDC 66715684600
RxCUI 1942710
UNII BBX060AN9V
UPC 0366715684608
Application # 505G(a)(3)
SPL Set ID 95408b83-b279-4738-a6d8-cbc626c17510
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-12-01
Route TOPICAL
Dosage form LIQUID
Substance HYDROGEN PEROXIDE
Quick answers
  • RxCUI (RxNorm): 1942710
Why two NDCs? The FDA registers this code as 66715-6846-0 — 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 → 66715-6846-00. 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 Antiinfectives and antiseptics for local oral treatment class.

Drug family (ATC) Antiinfectives and antiseptics for local oral treatment, Other antiseptics and disinfectants, Other dermatologicals
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

🧪 What is this product?

This is an over-the-counter topical liquid containing hydrogen peroxide at a 3% concentration. Hydrogen peroxide is commonly used as an antiseptic and cleansing agent on minor cuts, scrapes, and wounds. The product is marketed as an OTC monograph drug, meaning it follows the FDA's established safety and effectiveness rules for this category of topical antiseptics rather than being individually reviewed.

Supplement & herbal interactions

Some supplements/herbs that may interact with Hydrogen Peroxide — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Hydrogen Peroxide (3 interactions) — ranked by severity →
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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
66715-6846-00 You're viewing this Main listing 473 mL in 1 BOTTLE, PLASTIC 2016-08-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Hydrogen Peroxide 3 Percent 3 mL/100mL 70000-0500-01 Cardinal 946 ml $0.002 — Availability likely —
Hydrogen Peroxide 3 mL/100mL 70000-0022-01 Cardinal 236 ml $0.006 — Availability likely —
Hydrogen Peroxide Lil Drug Store Products 3 mL/100mLthis 66715-6846-00 Lil' 473 ml — — FDA listed —
Aplicare Hydrogen Peroxide 3 mL/100mL 52380-0013-01 Aplicare 30 ml — — Discontinued —
Aplicare 3 mL/100mL 52380-1013-03 Aplicare 30 ml — — FDA listed —
Hydrogen Peroxide 3 mL/100mL 70082-0111-16 DealMed 473 ml — — FDA listed —
Hydrogen Peroxide 3 mL/100mL 87251-0004-16 4 236 ml — — FDA listed —
Everlit Care Products Antiseptic Mist 3 mL/100mL 43473-0112-01 Nantong 59 ml — — FDA listed —
Florona Actilife Hydrogen Peroxide 3 % 3 mL/100mL 85891-0006-01 SPARROW 473 ml — — Discontinued —
Hydrogen Peroxide 3 mL/100mL 10565-0001-04 Hydrox 118 ml — — FDA listed —
3% Hydrogen Peroxide 3 mL/100mL 52000-0433-16 Universal 473 ml — — FDA listed —
Hydrogen Peroxide First Aid Antiseptic 3 mL/100mL 53329-0981-06 Medline 473 ml — — FDA listed —
HCS Hydrogen Peroxide 3% 3 mL/100mL 83506-0001-04 Concordance 118 ml — — FDA listed —
Everlit Care Products Antiseptic Mist 3 mL/100mL 83807-0033-01 EVERLIT 59 ml — — FDA listed —
Hydrogen Peroxide 3 mL/100mL 53943-0099-32 Discount 946 ml — — FDA listed —
3% Hydrogen Peroxide 3 mL/100mL 84809-0005-01 LJ 12 bottles — — FDA listed —
Hydrogen Peroxide 3 Percent ReadyInCase 3 mL/100mL 49580-0268-03 P 946 ml — — FDA listed —
Hydrogen Peroxide 3 mL/100mL 51316-0268-16 CVS 473 ml — — FDA listed —
Hydrogen Peroxide 3 mL/100mL 61734-0010-01 Delon 473 ml — — FDA listed —
Hydrogen Peroxide 3 mL/100mL 67751-0001-04 Navajo 118 ml — — FDA listed —
Hydrogen Peroxide 3 mL/100mL 49580-0400-03 P 946 ml — — FDA listed —
Pharmacys Prescription Hydrogen Peroxide 3 mL/100mL 72197-0051-16 American 473 ml — — 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
Dec 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.

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.

Manufacturer & labeler

LabelerLil' Drug Store Products, Inc
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code66715
First marketedDec 2014
Product typeHuman Otc Drug
Portfolio27 products on file

More NDCs from Lil' Drug Store Products, Inc labeler code 66715

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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

Uses first aid to help prevent the risk of infection in minor cuts, scrapes, and burns aids in the removal of phlegm, mucus, or other secretions associated with occasional sore mouth

⏱️ Dosage and Administration 123 words ▾

Directions For use as a first aid antiseptic: clean affected area if bandaged, let dry first apply small amount of product on affected area 1-3 times a day may be covered with a sterile bandage For use as an oral debriding agent (oral rinse): adults and children 2 years of age and over: mix with an equal amount of water swish around in the mouth over affected area for at least 1 minute and then spit out. Do not swallow. use up to 4 times daily after meals and at bedtime or as directed by a dentist or doctor children under 12 years should be supervised in the use of this product children under 2 years of age: consult a doctor or dentist

⚠️ Warnings 93 words ▾

Warnings For external use only. Do not use in the eyes or apply over large areas of the body longer than one week Ask a doctor before use if you have deep puncture wounds, animal bites or serious burns Stop use and ask a doctor if swelling, rash, or fever develops the condition persists or gets worse sore mouth symptoms do not improve in 7 days irritation, pain, or redness persists or worsens Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📦 Storage and Handling 23 words ▾

Other information keep tightly closed and in a dark place at room temperature do not shake bottle. Hold away from face when opening.

🧪 Active Ingredient 5 words ▾

Active ingredient Hydrogen peroxide 3%

🧪 Inactive Ingredients 4 words ▾

Inactive ingredient purified water

🎯 Purpose 6 words ▾

Purpose First aid antiseptic/oral debriding agent

📄 Do Not Use 18 words ▾

Do not use in the eyes or apply over large areas of the body longer than one week

📄 Ask a Doctor Before Use If 16 words ▾

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

📄 Stop Use and Ask a Doctor If 34 words ▾

Stop use and ask a doctor if swelling, rash, or fever develops the condition persists or gets worse sore mouth symptoms do not improve in 7 days irritation, pain, or redness persists or worsens

📄 Keep Out of Reach of Children 20 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📄 Questions or Comments 5 words ▾

Questions? 1-877-507-6516 (M-F 8AM-4:30PM CST)

📄 Package Label / Principal Display Panel 78 words ▾

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label QUALITY GUARANTEED Hydrogen Peroxide, 3% USP First Aid Antiseptic/Oral Debriding Agent For treatment of Minor Cuts & Scrapes Burns For use as a rinse of a Sore Mouth Product manufactured for: Lil' Drug Store Products, Inc. 1201 Continental Place NE Cedar Rapids, IA 52402 Questions? 1-877-507-6516 (M-F 8AM-4:30PM CST) 16 FL OZ (1 PT) 473 mL Lil' DrugStore ® 68460L-US-04-16 PLD-B220C LB004023 PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

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 Hydrogen Peroxide Lil Drug Store Products (this brand).

Top reported reactions

Nausea23
Fatigue22
Vomiting17
Headache16
Rash16
Pruritus14
Shock Haemorrhagic14

Age at onset

Neonate1
Child2
Adolescent2
Adult36
Elderly17

Reporter sex

0 reports
Male · 49%
Female · 49%
Unknown · 2%

Serious outcomes

Hospitalization127
Death43
Life-threatening31
Disabling7
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 40 14
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 — Not published for this NDC No photo available yet for this listing.
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 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 Lil' Drug Store Products, Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Lil' Drug Store Products, 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.
← 66715-6845-00 · Lil' 66715-6855-04 · Lil' →
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.