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Iodine 20 mg/mL Liquid, 30 mL — NDC 00363-0088-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Iodine 20 mg/mL Liquid, 30 mL — NDC 0363-0088-10 (Billing 00363-0088-10)

by Walgreen Co. · 30 mL in 1 BOTTLE, PLASTIC

This is a package of 30 mL of Iodine 20 mg/mL Liquid from Walgreen Co., marketed since Mar 2011 and currently FDA-listed. It is this product's only package size.

NDC 00363-0088-10
🏷️ FDA NDC (as labeled) 0363-0088-10 billing pads the labeler 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 0363-0088-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0363 labeler · 0088 product · 10 package
Package marketed since
Mar 11, 2011
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 0363008810 4
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0363-0088-10
Product NDC 0363-0088
11-digit billing NDC 00363008810
RxCUI 311093
UNII 9679TC07X4
Application # M003
SPL Set ID d3d44c9f-4eb6-4e5b-9943-c0f80f06952d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-03-11
Route TOPICAL
Dosage form LIQUID
Substance IODINE

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

GPI-14 41550030001220
GPI class Wal-itin
Quick answers
  • GPI-14 (Medi-Span): 41550030001220
  • RxCUI (RxNorm): 311093
Why two NDCs? The FDA registers this code as 0363-0088-10 — a 4-4-2 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 labeler segment → 00363-0088-10. 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 Iodine products class.

Drug family (ATC) Iodine products
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 a topical liquid containing iodine, an over-the-counter antiseptic product sold under FDA's monograph rules for skin antiseptics. Iodine is typically used as a topical disinfectant to help reduce bacteria and other microorganisms on the skin. This concentration (20 mg/mL) is commonly applied to minor cuts, scrapes, and other small wounds before bandaging or as part of skin preparation before medical procedures.

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
00363-0088-10 You're viewing this Main listing 30 mL in 1 BOTTLE, PLASTIC 2011-03-11 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Foster and Thrive 2% Mild Iodine Tincture 24 mg/mL; 20 mg/mL 70677-1204-01 Strategic 30 ml $0.072 — Availability likely —
Sunmark Iodine 20 mg/mL; 470 mg/mL; 24 mg/mL 49348-0133-27 Strategic 30 ml $0.072 — FDA listed —
Iodine 20 mg/mLthis 00363-0088-10 Walgreen 30 ml — — FDA listed —
Iodine 20 mg/mL 11344-0880-10 Nice-Pak 30 ml — — FDA listed —
Iodine Tincture 20 mg/mL 30142-0088-10 The 30 ml — — FDA listed —
Iodine 20 mg/mL 41163-0088-10 United 30 ml — — FDA listed —
mild iodine tincture 20 mg/mL; 470 mg/mL; 20.4 mg/mL 59450-0030-36 KROGER 30 ml — — FDA listed —
Salicylic Iodine (Iodo Salicilico) First Aid Antiseptic 20 mg/mL 73635-1220-01 Germa 30 ml — — FDA listed —
Iodine Tincture (IODO) First Aid Antiseptic 20 mg/mL 73635-1221-01 Germa 30 ml — — FDA listed —
Iodo Blanco (Iodine Tincture Decolorized) First Aid Antiseptic 20 mg/mL 73635-1222-01 Germa 30 ml — — FDA listed —
Iodine Tincture 20 mg/mL 76162-0088-10 Topco 30 ml — — FDA listed —
Ioddo Iodine .56 g/28g 84178-0005-03 EVI 28 g — — 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

🏛️
2011
On the market since
Mar 2011
📍
2026
Currently FDA-listed
15 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII F5WR8N145C
    Sodium iodide is an inorganic salt containing iodine. In medications, it acts as a source of iodine and may serve as a preservative or stabilizer to help maintain product quality and shelf life.
  • 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.

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

The official label also statesalcohol (47%v/v), purified water, sodium iodide

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

LabelerWalgreen Co.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code00363
First marketedMar 2011
Product typeHuman Otc Drug
Portfolio132 products on file

More NDCs from Walgreen Co. labeler code 00363

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 🤒 Adverse Reactions 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Use First aid to help prevent skin infection in minor cuts scrapes burns

⏱️ Dosage and Administration 29 words ▾

Directions clean the affected area apply a small amount on the area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first

⚠️ Warnings 5 words ▾

Warnings For external use only

🤒 Adverse Reactions 29 words ▾

ADVERSE REACTION Walgreen Pharmacist Recommended Our Pharmacists recommend the Walgreens brand. Distributed by: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015 100% satisfaction guaranteed walgreens.com 1-800-925-4733 2021 Walgreen Co.

🧪 Active Ingredient 4 words ▾

Active Ingredient Iodine 2%

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients alcohol (47%v/v), purified water, sodium iodide

🎯 Purpose 4 words ▾

Purpose First aid antiseptic

📄 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.

📄 When Using This Product 29 words ▾

When using this product do not use in eyes or apply over large areas of the body do not use longer than 1 week unless directed by a doctor

📄 Stop Use and Ask a Doctor If 12 words ▾

Stop use and ask a doctor if condition persists or gets worse

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 33 words ▾

principal display panel Walgreens Iodine tincture USP First aid antiseptic For external use only Helps to prevent skin infection in minor cuts, scrapes, burns CAUTION: POISON 1 FL OZ (30 mL) image description

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 Iodine — the ingredient across all brands.

Top reported reactions

Drug Hypersensitivity1,458
Nausea697
Fatigue570
Diarrhoea531
Dyspnoea519
Headache502
Rash494

Age at onset

Neonate39
Infant19
Child10
Adolescent10
Adult532
Elderly475

Reporter sex

8,174 reports
Male · 30%
Female · 70%
Unknown · 0%
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 763 0
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 Walgreen Co.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Walgreen Co. 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.
← 00363-0085-34 · Walgreen 00363-0092-08 · Walgreens →
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.