Home › NDC Lookup › Ingredients › Povidone Iodine, Isopropyl Alcohol › 84128-0012-30
🧽image loading
(from DailyMed)

Swab Applicator Brushes Iodine (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) Povidone Iodine, 100 mg/mL; 740 mg/mL Swab — NDC 84128-012-30 (Billing 84128-0012-30)

by XINXIANG XINDA TECHNOLOGY CO.,LTD · 10 BAG in 1 BOX / 1 APPLICATOR in 1 BAG / 30 mL in 1 APPLICATOR

This is a package of Swab Applicator Brushes Iodine (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) Povidone Iodine, 100 mg/mL; 740 mg/mL Swab from XINXIANG XINDA TECHNOLOGY CO.,LTD, no longer marketed (first marketed Jun 2026), no longer in the FDA NDC Directory.

NDC 84128-0012-30
🏷️ FDA NDC (as labeled) 84128-012-30 billing pads the product segment with a zero
This package
Contains30 mL in 1 applicator Pack sizes6 compare ↓
Product page 84128-0012-03 Also comes in: 3 mL 84128-012-03 6 mL 84128-012-06 10.5 mL 84128-012-10 26 mL 84128-012-26 35 mL 84128-012-35
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jun 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 84128-012-30 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84128 labeler · 012 product · 30 package
Package marketed since
Jun 11, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
6977191590495, 6977191590471, 6977191590457, 6977191590464 +1 more
FDA record last changed
Jun 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Jun 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84128-012-30
Product NDC 84128-012
11-digit billing NDC 84128001230
UNII 6E43AWY083, ND2M416302
UPC 6977191590495, 6977191590471, 6977191590457, 6977191590464 +1 more
Application # M003
SPL Set ID 53f502fd-21f5-dfb8-e063-6394a90a1116
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Jun 2026)
Marketing start 2026-06-11
Route TOPICAL
Dosage form SWAB
Substance IODINE POVACRYLEX; ISOPROPYL ALCOHOL
Why two NDCs? The FDA registers this code as 84128-012-30 — 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 → 84128-0012-30. 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

🧪 What is this product?

This is a topical swab product containing povidone iodine (iodine povacrylex) and isopropyl alcohol, marketed as an over-the-counter monograph drug. Povidone iodine is an iodine-based antiseptic commonly used to reduce microorganisms on the skin before medical procedures or for minor wound cleansing. Isopropyl alcohol functions as an antimicrobial agent and helps the solution dry quickly on the skin. The swab applicator format is designed for convenient application to small areas of skin.

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 eachPer 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.
Try another pack size: 3 mL 6 mL 10.5 mL 26 mL 35 mL
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
84128-0012-03 84128-012-03 Main listing 20 BAG in 1 BOX / 1 APPLICATOR in 1 BAG / 3 mL in 1 APPLICATOR 2026-06-11 — Discontinued by firm
84128-0012-06 84128-012-06 20 BAG in 1 BOX / 1 APPLICATOR in 1 BAG / 6 mL in 1 APPLICATOR 2026-06-11 — Discontinued by firm
84128-0012-10 84128-012-10 10 BAG in 1 BOX / 1 APPLICATOR in 1 BAG / 10.5 mL in 1 APPLICATOR 2026-06-11 — Discontinued by firm
84128-0012-26 84128-012-26 10 BAG in 1 BOX / 1 APPLICATOR in 1 BAG / 26 mL in 1 APPLICATOR 2026-06-11 — Discontinued by firm
84128-0012-30 You're viewing this 10 BAG in 1 BOX / 1 APPLICATOR in 1 BAG / 30 mL in 1 APPLICATOR 2026-06-11 — Discontinued by firm
84128-0012-35 84128-012-35 10 BAG in 1 BOX / 1 APPLICATOR in 1 BAG / 35 mL in 1 APPLICATOR 2026-06-11 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 10 bag in 1 box / 1 applicator in 1 bag / 30 ml in 1 applicator.
What NDC number is used to bill for this package of Swab Applicator Brushes Iodine (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) Povidone Iodine, 100 mg/mL; 740 mg/mL Swab?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Swab Applicator Brushes Iodine (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) 100 mg/mL; 740 mg/mLthis 84128-0012-30 XINXIANG 1 applicator — — Discontinued —
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

🏛️
2026
On the market since
Jun 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
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

LabelerXINXIANG XINDA TECHNOLOGY CO.,LTD
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code84128
First marketedJun 2026
Product typeHuman Otc Drug
Portfolio13 products on file

More NDCs from XINXIANG XINDA TECHNOLOGY CO.,LTD labeler code 84128

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 📄 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 21 words ▾

Use for the preparation of the patient's skin prior to surgery. Helps to reduce bacteria that potentially can cause skin infection.

⏱️ Dosage and Administration ~1 min read ▾

Directions Use with care in premature infants or infants under 2 months of age. These products may cause skin irritation or chemical burns. Use in a well ventilated area Maximal treatment area for one applicator is approximately 13.2 in. x 13.2 in.

(1126 cm²). Do not use 26-ml applicator for area smaller than 8.4 in. x 8.4 in. Use a smaller applicator instead.

Do not use 26-ml applicator for head and neck surgery Remove applicator from package; do not touch sponge hold the applicator with the sponge down. Open the switch only once to activate the ampules and release the antiseptic. Wet the sponge by pressing and releasing the sponge against the treatment area until liquid is visible on the skin Completely wet the treatment area with antiseptic Dry surgical sites (e.g. abdomen or arm): use gentle repeated back-and-forth strokes for 30 seconds Moist surgical sites (e.g., inguinal fold): use gentle repeated back-and-forth strokes for 2 minutes Do not allow solution to pool; tuck prep towels to absorb solution, and then remove Allow the solution to completely dry (minimum of 3 minutes on hairless skin; up to 1 hour in hair).

Do not blot or wipe away. Discard the applicator after a single use along with any portion of the solution not required to cover the prep area. It is not necessary to use the entire amount available.

⚠️ Warnings 204 words ▾

Warnings For external use only. Flammable, keep away from fire or flame. To reduce risk of fire, PREP CAREFULLY: Do not use 3-ml applicator for head and neck surgery Solution contains alcohol and gives off flammable vapors Avoid getting solution into hairy areas.

Hair may take up to 1 hour to dry. Wet hair is flammable Do not drape or use ignition source (e.g., cautery, laser) until solution is completely dry (minimum of 3 minutes on hairless skin; up to 1 hour in hair) Do not allow solution to pool Remove wet materials from prep area Do not use On patients with known allergies to Iodine or isopropyl alcohol For lumbar puncture or in contact with the meninges On open skin wounds or as a general skin cleanser When using this product keep out of eyes, ears, and mouth. May cause serious or permanent injury if permitted to enter and remain.

If contact occurs, rinse with cold water right away and contact a doctor. Stop use and ask a doctor if irritation, sensitization, or allergic reaction occurs. These may be signs of a serious condition.

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

📦 Storage and Handling 13 words ▾

Other information Store between 15-30°C (59-86°F) avoid freezing and excessive heat above 40°C(104°F)

🧪 Active Ingredient 10 words ▾

Active ingredients Iodine (0.7% Available Iodine) Isopropyl alcohol 74% w/w

🧪 Inactive Ingredients 5 words ▾

Inactive ingredients USP Purified water

🎯 Purpose 2 words ▾

Purposes Antiseptic

📄 Do Not Use 32 words ▾

Do not use On patients with known allergies to Iodine or isopropyl alcohol For lumbar puncture or in contact with the meninges On open skin wounds or as a general skin cleanser

📄 When Using This Product 36 words ▾

When using this product keep out of eyes, ears, and mouth. May cause serious or permanent injury if permitted to enter and remain. If contact occurs, rinse with cold water right away and contact a doctor.

📄 Stop Use and Ask a Doctor If 21 words ▾

Stop use and ask a doctor if irritation, sensitization, or allergic reaction occurs. These may be signs of a serious condition.

📄 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 12 words ▾

84128-012-03 3ml

84128-012-06 6ml

84128-012-10 10.5ml

84128-012-26 26ml

84128-012-30 30ml

84128-012-35 35ml

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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 5 other package presentations of this same product, including 1 applicator (84128-0012-03), 1 applicator (84128-0012-06), 1 applicator (84128-0012-10). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
XINXIANG XINDA TECHNOLOGY CO.,LTD 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.
← 84128-0011-01 · XINXIANG 84128-0013-01 · Xinxiang →
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.