Home › NDC Lookup › Ingredients › Model Aa-2012 › 27860-0014-01
Model AA-2012 Kit — NDC 27860-0014-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Model AA-2012 Kit — NDC 27860-014-01 (Billing 27860-0014-01)

by AEROSPACE ACCESSORY SERVICE · 1 KIT in 1 KIT * 2.6 g in 1 PACKET * 100 PACKET in 1 BOX / .55 mL in 1 PACKET

This is a package of Model AA-2012 Kit from AEROSPACE ACCESSORY SERVICE, marketed since Jun 2022 and currently FDA-listed. It is this product's only package size.

NDC 27860-0014-01
🏷️ FDA NDC (as labeled) 27860-014-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 27860-014-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
27860 labeler · 014 product · 01 package
Package marketed since
Jun 1, 2022
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0616784130323
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 27860-014-01
Product NDC 27860-014
11-digit billing NDC 27860001401
RxCUI 1038558
UPC 0616784130323
Application # M003
SPL Set ID e29b0f92-27b7-e09f-e053-2995a90a35e3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-06-01
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 1038558
Why two NDCs? The FDA registers this code as 27860-014-01 — 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 → 27860-0014-01. 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 Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
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?

Model AA-2012 KIT is an over-the-counter monograph product sold as a kit. The specific active ingredients are not listed in this directory entry, so the exact contents and intended use cannot be determined from the information provided. To learn what this kit contains and what it is typically used for, consult the product packaging, label, or manufacturer information.

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.
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
27860-0014-01 You're viewing this Main listing 1 KIT in 1 KIT * 2.6 g in 1 PACKET * 100 PACKET in 1 BOX / .55 mL in 1 PACKET 2022-06-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Model AA-2012this 27860-0014-01 AEROSPACE 1 kit — — 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

🏛️
2022
On the market since
Jun 2022
📍
2026
Currently FDA-listed
4 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.

What it looks like

ShapeRectangle
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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.

From the label’s inactive-ingredient sectionPurified water

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

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

LabelerAEROSPACE ACCESSORY SERVICE
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code27860
First marketedJun 2022
Product typeHuman Otc Drug
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 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 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 22 words ▾

Antiseptic Wipes Uses First Aid Antiseptic

BZK Pads Uses First aid to help prevent skin infection in minor cuts, scrapes and burns

⏱️ Dosage and Administration 61 words ▾

Antiseptic Wipes Directions Tear open pouch and use as part of your daily cleansing routine. Clean the affected area. Apply this product on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

BZK Pads Directions Clean the affected area May be covered with a sterile bandage If bandaged, let dry first

⚠️ Warnings 161 words ▾

Antiseptic Wipes Warnings For external use only Do not use Do not use it in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Stop use and consult a doctor if the condition persists or gets worse.

Do not use it for longer than 1 week unless directed by a doctor. Antiseptic Wipes Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

BZK Pads Warnings For external use only Do not use As an antiseptic for more than 1 week In the eyes Ask a Doctor before use if you have deep puncture wounds, animal bites, or serious burns Stop use and ask a doctor if irritation or redness develop Condition persistor gets worse Keep out of reach of children If swallowed get medical help or contact a Poison Control Center ( 1-800-222-1222) right away

🧪 Active Ingredient 16 words ▾

Antiseptic Wipes Active ingredient Benzalkonium Chloride 0.13% v/v

BZK Pads Active ingredient Benzalkonium Chloride 0.13% v/v

🧪 Inactive Ingredients 6 words ▾

Antiseptic Wipes Inactive ingredients Purified water

🎯 Purpose 12 words ▾

Antiseptic Wipes Purpose First Aid Antiseptic

BZK Pads Purpose First Aid Antiseptic

📄 Do Not Use 74 words ▾

Do not use Do not use it in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Stop use and consult a doctor if the condition persists or gets worse. Do not use it for longer than 1 week unless directed by a doctor.

Do not use As an antiseptic for more than 1 week In the eyes

📄 Ask a Doctor Before Use If 16 words ▾

Ask a Doctor before use if you have deep puncture wounds, animal bites, or serious burns

📄 Stop Use and Ask a Doctor If 15 words ▾

Stop use and ask a doctor if irritation or redness develop Condition persistor gets worse

📄 Keep Out of Reach of Children 42 words ▾

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

Keep out of reach of children If swallowed get medical help or contact a Poison Control Center ( 1-800-222-1222) right away

📄 Other Information 44 words ▾

Antiseptic Wipes Other information store at room temperature between 59-86 F If contact with eyes occurs, flush eyes with water

BZK Pads Other Information Store at room temperature 15-30C (59-86F) Avoid excessive heat Temper evident. Do not use if packet is torn or cut

📄 Questions or Comments 20 words ▾

Antiseptic Wipes Questions Call 1-866-322-4634, weekdays between 8:00 am and 6:00 pm EST

BZK Pads Questions 1-800-DYNAREX Monday-Friday 9AM-5PM EST

📄 Package Label / Principal Display Panel 15 words ▾

Antiseptic Wipes Principal Display Panel label

BZK Pads Principal Display Panel label

Model AA-2012 label

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 Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 AEROSPACE ACCESSORY SERVICE. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
AEROSPACE ACCESSORY SERVICE 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.
← 27854-0777-99 · Belmora 28105-0421-40 · HILL →
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.