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Foster and Thrive 2% Mild Iodine Tincture Iodine and Sodium Iodide and Alcohol Liquid 24 mg/mL; 20 mg/mL Liquid, 30 mL — NDC 70677-1204-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Foster and Thrive 2% Mild Iodine Tincture Iodine and Sodium Iodide and Alcohol Liquid 24 mg/mL; 20 mg/mL Liquid, 30 mL — NDC 70677-1204-1 (Billing 70677-1204-01)

by Strategic Sourcing Services, LLC · 30 mL in 1 BOTTLE, PLASTIC

This is a package of 30 mL of Foster and Thrive 2% Mild Iodine Tincture Iodine and Sodium Iodide and Alcohol Liquid 24 mg/mL; 20 mg/mL Liquid from Strategic Sourcing Services, LLC, marketed since Dec 2024 and currently FDA-listed; retail pharmacies pay about $0.0719 per mL (NADAC). It is this product's only package size.

NDC 70677-1204-01
🏷️ FDA NDC (as labeled) 70677-1204-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 →

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 70677-1204-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
70677 labeler · 1204 product · 1 package
Package marketed since
Dec 17, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Billing quantity
30 mL per package
Barcode (UPC-A, from the NDC)
3 7067712041 8
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70677-1204-1
Product NDC 70677-1204
11-digit billing NDC 70677120401
NCPDP billing unit ML — per mL (volume)
RxCUI 311093
UNII F5WR8N145C, 9679TC07X4
Application # M003
SPL Set ID 2981cb97-17de-ebda-e063-6394a90ad281
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-12-17
Route TOPICAL
Dosage form LIQUID
Substance SODIUM IODIDE; IODINE

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

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 FT IODINE 2% TINCTURE
FDB brand name Iodine
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 062671
  • GCN: 98445
  • HICL (First Databank): 005095
  • AHFS class code: 84:04.16.00
  • RxCUI (RxNorm): 311093
Why two NDCs? The FDA registers this code as 70677-1204-1 — 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 → 70677-1204-01. 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

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

Foster and Thrive 2% Mild Iodine Tincture is a topical liquid product containing iodine and sodium iodide. This combination is typically used as an antiseptic on skin. Iodine has long been applied to minor cuts, scrapes, and wounds to help reduce bacteria on the skin surface. This is an OTC monograph product, meaning it is marketed under FDA's established rulebook for this category of antimicrobial skin products rather than as an individually approved application.

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 2025 Mar 2026 Jun 2026 Sep 2026 $0.076 $0.068
▼ Down 6% over the last 10 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
70677-1204-01 You're viewing this Main listing 30 mL in 1 BOTTLE, PLASTIC 2024-12-17 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Foster and Thrive 2% Mild Iodine Tincture 24 mg/mL; 20 mg/mLthis 70677-1204-01 Strategic 30 ml $0.072 — Availability likely —
LEADER 2% Mild Iodine Tincture 24 mg/mL; 20 mg/mL 70000-0401-01 Cardinal 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 +0%
Iodine 20 mg/mL 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

🏛️
2024
On the market since
Dec 2024
📍
2026
Currently FDA-listed
2 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 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.

2 inactive ingredients 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

LabelerStrategic Sourcing Services, LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code70677
First marketedDec 2024
Product typeHuman Otc Drug
Portfolio24 products on file

More NDCs from Strategic Sourcing Services, LLC labeler code 70677

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 12 words ▾

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

⏱️ Dosage and Administration 28 words ▾

Clearn the affected area apply a small amount to the affected area 1 to 3 times daily. May be covered with sterile bandage. If bandaged let dry first.

⚠️ Warnings 11 words ▾

For external use only. Flammable, keep away from fire and flame

🧪 Active Ingredient 4 words ▾

Iodine Tincture USP 2%

🧪 Inactive Ingredients 2 words ▾

Purified Water

🎯 Purpose 3 words ▾

First Aid 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 lids Do not apply over large areas of the body

📄 Stop Use and Ask a Doctor If 25 words ▾

Stop use and ask a doctor if the condition persists or gets worse Do not use longer than 1 week unless directed by a doctor

📄 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 immediately. (1-800-222-1222)

📄 Package Label / Principal Display Panel 3 words ▾

FT Mild Iodine

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 70677-1202-01 · Strategic 70677-1207-02 · Strategic →
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.