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GNP Idoinde Tincture 2% Mild Iodine and Sodium Iodide and Alcohol 20 mg/mL; 20.4 mg/mL; 470 mg/mL Liquid, 30 mL — NDC 24385-0213-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

GNP Idoinde Tincture 2% Mild Iodine and Sodium Iodide and Alcohol 20 mg/mL; 20.4 mg/mL; 470 mg/mL Liquid, 30 mL — NDC 24385-213-10 (Billing 24385-0213-10)

by Amerisource Bergen · 30 mL in 1 BOTTLE, PLASTIC

This is a package of 30 mL of GNP Idoinde Tincture 2% Mild Iodine and Sodium Iodide and Alcohol 20 mg/mL; 20.4 mg/mL; 470 mg/mL Liquid from Amerisource Bergen, marketed since Jan 2008 and currently FDA-listed; retail pharmacies pay about $0.0719 per mL (NADAC). It is this product's only package size.

NDC 24385-0213-10
🏷️ FDA NDC (as labeled) 24385-213-10 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 Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

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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 24385-213-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
24385 labeler · 213 product · 10 package
Package marketed since
Nov 16, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Billing quantity
30 mL per package
Barcode (UPC)
0087701403903
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 24385-213-10
Product NDC 24385-213
11-digit billing NDC 24385021310
NCPDP billing unit ML — per mL (volume)
UNII 9679TC07X4, F5WR8N145C, 3K9958V90M
UPC 0087701403903
Application # M003
SPL Set ID 32ad75b8-abd1-4151-a035-b6c9ae5fc888
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2008-01-01
Route TOPICAL
Dosage form LIQUID
Substance IODINE; SODIUM IODIDE; ALCOHOL

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

GPI-14 92200020001510
GPI class GNP Iodine
GCN Seq No 062671
GCN 98445
HICL code 005095
Ingredient (HICL) Iodine/Sodium Iodide
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5B
Therapeutic class — specific (HIC3) Topical Preparations,Antibacterials
AHFS code 84:04.16.00
AHFS class Astringents, Anti-Infective
FDB label name IODINE 2% MILD TINCTURE
FDB brand name Iodine
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 062671
  • GCN: 98445
  • GPI-14 (Medi-Span): 92200020001510
  • HICL (First Databank): 005095
  • AHFS class code: 84:04.16.00
Why two NDCs? The FDA registers this code as 24385-213-10 — 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 → 24385-0213-10. 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.

Clinical

Label name IODINE 2% MILD TINCTURE Ingredient Iodine/Sodium Iodide
🧪 What is this product?

GNP Idoinde Tincture is a topical liquid containing iodine and sodium iodide as active ingredients, marketed as an over-the-counter monograph product. Iodine and sodium iodide are halogens typically used in topical antiseptic and antimicrobial preparations. This product is applied directly to the skin and is commonly found in first-aid settings as a disinfectant for minor cuts, scrapes, and wound care. The alcohol content in the formulation serves as an additional antimicrobial and drying agent.

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 $0.072 $2.16 / 30 ml
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.
NADAC price history (per mL) — tap or hover for the price & month
Dec 2021 Aug 2022 Feb 2026 Sep 2026 $0.079 $0.066
▲ Up 9% over the last 22 months.
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
24385-0213-10 You're viewing this Main listing 30 mL in 1 BOTTLE, PLASTIC 2017-11-16 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
GNP Idoinde Tincture 2% Mild 20 mg/mL; 20.4 mg/mL; 470 mg/mLthis 24385-0213-10 Amerisource 30 ml $0.072 — Availability likely —
Health Mart Iodine Tincture Mild 20 mg/mL; 20.4 mg/mL; 470 mg/mL 62011-0117-01 Strategic 30 ml $0.072 — FDA listed +0%
De La Cruz Tincture of Iodine 20 mg/mL; 20.4 mg/mL; 470 mg/mL 24286-1528-07 DLC 30 ml — — FDA listed —
DDM Iodine Tincture Mild 20 mg/mL; 20.4 mg/mL; 470 mg/mL 53943-0213-91 Discount 30 ml — — FDA listed —
Quality Choice Iodine Tincture Mild 20 mg/mL; 20.4 mg/mL; 470 mg/mL 63868-0330-01 Chain 30 ml — — FDA listed —
Harris Teeter Iodine Tincture Mild 20 mg/mL; 20.4 mg/mL; 470 mg/mL 69256-0213-91 Harris 30 ml — — FDA listed —
Iodine Tincture Mild 20 mg/mL; 20.4 mg/mL; 470 mg/mL 00395-1213-16 Humco 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

🏛️
2008
On the market since
Jan 2008
📍
2026
Currently FDA-listed
18 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

LabelerAmerisource Bergen
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code24385
First marketedJan 2008
Product typeHuman Otc Drug
Portfolio206 products on file

More NDCs from Amerisource Bergen labeler code 24385

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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Uses: To help prevent infection in minor cuts, scrapes and burns.

⏱️ Dosage and Administration 29 words ▾

Directions: Clean the affected area. Apply a small amount to the affeted area 1 to 3 times daily. May be covered with sterile bandage. If bandaged, let dry first.

⚠️ Warnings 5 words ▾

Warnings: For external use only

🧪 Active Ingredient 9 words ▾

Active Ingredients Iodine 2% Sodium iodide 2.4% Alcohol 47%

🧪 Inactive Ingredients 4 words ▾

Inactive ingredient: Purified Water.

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Ask a Doctor Before Use If 16 words ▾

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

📄 When Using This Product 33 words ▾

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

📄 Stop Use and Ask a Doctor If 22 words ▾

Stop use and ask a doctor if condition persists or gets worse, or if using this product for longer than 1 week.

📄 Keep Out of Reach of Children 37 words ▾

Keep out of reach ofchildren In case of accidental ingestion, give milk then give 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 16 words ▾

Other information: Will stain skin and clothing Dist. by: AmerisourceBergen 1300 Morris Dr., Chesterbrook, PA 19087

📄 Questions or Comments 5 words ▾

Questions or Comments? 1-800-662-3435 www.goodneighborpharmacy.com

📄 Package Label / Principal Display Panel 35 words ▾

Principal Display Panel Good Neighbor Pharmacy NDC 24385-0213-10 Iodine Tincture USP 2% Mild Antiseptic First Aid First Aid Antiseptic Alcohol 47% FLAMMABLE: Keep away from sparks, heal & flame. 1 FL OZ (30 mL) label

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 24385-0210-03 · Amerisource 24385-0267-10 · AMERISOURCE →
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.