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Iodine Tincture Mild Iodine and Sodium Iodide and Alcohol 20.4 mg/mL; 470 mg/mL; 20 mg/mL Liquid, 30 mL — NDC 82645-0911-91 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Iodine Tincture Mild Iodine and Sodium Iodide and Alcohol 20.4 mg/mL; 470 mg/mL; 20 mg/mL Liquid, 30 mL — NDC 82645-911-91 (Billing 82645-0911-91)

by Pharma Nobis, LLC · 30 mL in 1 BOTTLE

This is a package of 30 mL of Iodine Tincture Mild Iodine and Sodium Iodide and Alcohol 20.4 mg/mL; 470 mg/mL; 20 mg/mL Liquid from Pharma Nobis, LLC, marketed since Jan 1979 and currently FDA-listed. It is this product's only package size.

NDC 82645-0911-91
🏷️ FDA NDC (as labeled) 82645-911-91 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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 82645-911-91 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
82645 labeler · 911 product · 91 package
Package marketed since
Nov 14, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0840986012983, 0635515992054, 0011110355492, 0079068000864 +10 more
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82645-911-91
Product NDC 82645-911
11-digit billing NDC 82645091191
RxCUI 311093
UNII F5WR8N145C, 3K9958V90M, 9679TC07X4
UPC 0840986012983, 0635515992054, 0011110355492, 0079068000864 +10 more
Application # M003
SPL Set ID e42df0bf-cce7-3961-e053-2995a90a730a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1979-01-01
Route TOPICAL
Dosage form LIQUID
Substance SODIUM IODIDE; ALCOHOL; IODINE
Quick answers
  • RxCUI (RxNorm): 311093
Why two NDCs? The FDA registers this code as 82645-911-91 — 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 → 82645-0911-91. 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 iodine product sold over the counter under FDA's monograph rules for antiseptic skin preparations. The active ingredients are iodine and sodium iodide, which are typically used as antimicrobial agents on skin, and alcohol, which functions as a solvent and antiseptic. This type of product is commonly applied to minor cuts, scrapes, and wounds as a topical disinfectant.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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
82645-0911-91 You're viewing this Main listing 30 mL in 1 BOTTLE 2017-11-14 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Iodine Tincture Mild 20.4 mg/mL; 470 mg/mL; 20 mg/mLthis 82645-0911-91 Pharma 30 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

🏛️
1979
On the market since
Jan 1979
📍
2026
Currently FDA-listed
47 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 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesPurified 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 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

LabelerPharma Nobis, LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code82645
First marketedJan 1979
Product typeHuman Otc Drug
Portfolio40 products on file

More NDCs from Pharma Nobis, LLC labeler code 82645

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 🧪 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 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Indications First aid to help prevent infection in minor cuts, scrapes and burns

⏱️ Dosage and Administration 28 words ▾

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

⚠️ Warnings 123 words ▾

Warnings For external use only . Ask a doctor before use if you have deep or puncture wounds animal bites serious burns Flammable: Keep away from sparks heat and flame St op use and consult doctor if the condition persists or gets worse, or if using for longer than one week When using this product do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids do not apply over large areas of the body Keep out of reach of children .

In case of accidental ingestion, give milk then a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water. Contact a Poison Control Center immediately.

🧪 Active Ingredient 13 words ▾

Active ingredient Iodine 2%

Active ingredient Sodium Iodide 2.4%

Active ingredient Alcohol 47%

🧪 Inactive Ingredients 4 words ▾

Inactive ingredient Purified Water

🎯 Purpose 12 words ▾

Purpose First Aid Antiseptic

Purpose First Aid Antiseptic

Purpose First Aid Antiseptic

📄 Ask a Doctor Before Use If 24 words ▾

Ask a doctor before use if you have deep or puncture wounds animal bites serious burns Flammable: Keep away from sparks heat and flame

📄 When Using This Product 34 words ▾

When using this product do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids do not apply over large areas of the body

📄 Stop Use and Ask a Doctor If 21 words ▾

St op use and consult doctor if the condition persists or gets worse, or if using for longer than one week

📄 Keep Out of Reach of Children 38 words ▾

Keep out of reach of children . In case of accidental ingestion, give milk then a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water. Contact a Poison Control Center immediately.

📄 Other Information 7 words ▾

Other information will stain skin and clothing

📄 Package Label / Principal Display Panel 106 words ▾

Good Neighbor Label GNP

Leader Label LDRMild.jpg Leader

Quality Choice Label QC

Sunmark Label SMMild.jpg Sunmark

Premier Value Label PVMild.jpg PV

DDM Label DDM

De La Cruz Label DLCMild.jpg DLC

CVS Label CVS Iodine Tincture 12-30-22 CVS Iodine Old 1 CVS Iodine Old 2 CVS Iodine Old 3

Harris Teeter Label HT Iodine Tincture HT Iodine Tincture 2022

Kroger Label Kroger Mild Iodine 2026 KrogerMild.jpg Kroger

Safeway Label Safeway

Vida Mia Label VM

Swan Label SwanMild.jpg Swan

Good Sense Label GoodSenseMild.jpg Good Sense

Walgreen Label Walgreens Iodine 1 WallgreensMild.jpg Walgreen

Health Mart Label HM

Equaline Label EqualineMild.jpg Equaline

TopCare Iodine Tincture Top Care Iodine Tincture 12-30-22

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 Pharma Nobis, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Pharma Nobis, 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.
← 82645-0910-45 · Pharma 82645-0912-92 · Pharma →
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.