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Blood Clotting First Aid benzethonium chloride and lidocaine 3400 mg/85g; 170 mg/85g Aerosol, Spray, 85 g — NDC 47682-226-17 (Billing 47682-0226-17)

by Unifirst First Aid Corporation · 85 g in 1 BOTTLE, SPRAY

This is a package of 85 g of Blood Clotting First Aid benzethonium chloride and lidocaine 3400 mg/85g; 170 mg/85g Aerosol, Spray from Unifirst First Aid Corporation, marketed since Apr 2013 and currently FDA-listed. It is this product's only package size.

NDC 47682-0226-17
🏷️ FDA NDC (as labeled) 47682-226-17 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 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 47682-226-17
Product NDC 47682-226
11-digit billing NDC 47682022617
NCPDP billing unit GM — per gram (weight)
RxCUI 1545716
UNII 98PI200987, PH41D05744
UPC 0347682226176
Application # M003
SPL Set ID 2e544963-aa49-49cd-837e-9d89d86e257f
Established class (EPC) Amide Local Anesthetic; Antiarrhythmic
Physiologic effect Local Anesthesia
Chemical class Amides
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-04-05
Route TOPICAL
Dosage form AEROSOL, SPRAY
Substance LIDOCAINE; BENZETHONIUM CHLORIDE

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

GPI-14 90972000003200
GPI class Blood Clotting Spray
GCN Seq No 047809
GCN 13099
HICL code 022044
Ingredient (HICL) Lidocaine/Benzethon Cl
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 Q5H
Therapeutic class — specific (HIC3) Topical Local Anesthetics
AHFS code 72:00.00.00
AHFS class Local Anesthetics
FDB label name BLOOD CLOTTING SPRAY
FDB brand name Blood Clotting
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 047809
  • GCN: 13099
  • GPI-14 (Medi-Span): 90972000003200
  • HICL (First Databank): 022044
  • AHFS class code: 72:00.00.00
  • RxCUI (RxNorm): 1545716
Why two NDCs? The FDA registers this code as 47682-226-17 — 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 → 47682-0226-17. 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 Antiseptics class.

Drug family (ATC) Antiseptics, Quaternary ammonium compounds
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 BLOOD CLOTTING SPRAY Ingredient Lidocaine/Benzethon Cl
🧪 What is this product?

Blood Clotting First Aid is an over-the-counter topical spray sold under FDA's monograph rules for first aid products. It contains lidocaine, a local anesthetic that is typically used to numb minor pain and discomfort on the skin, and benzethonium chloride, an antimicrobial agent commonly used to help reduce bacteria on the skin surface. This aerosol spray form is applied directly to the affected area for minor wound care and first aid purposes.

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
47682-0226-17 You're viewing this Main listing 85 g in 1 BOTTLE, SPRAY 2013-04-05 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Super-Stop BloodClotter .2 mg/100mg; 4 mg/100mg 42961-0223-01 Cintas 85000 mg — — FDA listed —
Blood Clotting First Aid 3400 mg/85g; 170 mg/85gthis 47682-0226-17 Unifirst 85 g — — FDA listed —
Green Guard Super Stat Blood Clotting First Aid 3400 mg/85g; 170 mg/85g 47682-0300-17 Unifirst 85 g — — FDA listed —
Blood Clotting 3400 mg/85g; 170 mg/85g 50332-0217-01 HART 85 g — — FDA listed —
Redicare Blood Clotting 170 mg/85g; 3400 mg/85g 71105-0107-03 Redicare 85 g — — Discontinued —
Your Label Here Blood Clotting First Aid 3400 mg/85g; 170 mg/85g 52982-0106-03 Dixon 85 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

🏛️
2013
On the market since
Apr 2013
📍
2026
Currently FDA-listed
13 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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

LabelerUnifirst First Aid Corporation
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code47682
First marketedApr 2013
Product typeHuman Otc Drug
Portfolio183 products on file
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 📄 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 25 words ▾

Uses for help in control of superficial bleeding for temporary relief of pain and to help protect against infection in minor cuts, scrapes, and burns

⏱️ Dosage and Administration 54 words ▾

Directions clean the affected area shake can well before using hold 6-8 inches from surface spray until area is covered and superficial bleeding is stopped scab-like cover will gradually disappear or may be removed with soap and water for adult institutional use only not intended for use on children under 12 years of age

⚠️ Warnings 21 words ▾

Warnings For external use only Flammable keep away from fire or flame contents under pressure do not puncture or incinerate container

🧪 Active Ingredient 9 words ▾

Active Ingredients Benzethonium Chloride 0.2% w/w Lidocaine 4% w/w

🧪 Inactive Ingredients 13 words ▾

Inactive ingredients isobutane, isopropyl myristate, karaya, n-butane, propane, silica, sorbitan monooloate, talc, tragacanth.

🎯 Purpose 5 words ▾

Purpose Topical antiseptic Topical anesthetic

📄 Do Not Use 42 words ▾

Do not use in or near eyes or other mucus membranes in case of serious burns in case of deep or puncture wounds for a prolonged period of time on a large portion of the body on raw surfaces on blistered areas

📄 Stop Use and Ask a Doctor If 31 words ▾

Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days condition clears up and recurs within a few days redness, swelling, or irritation occurs

📄 Keep Out of Reach of Children 20 words ▾

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

📄 Other Information 35 words ▾

Other information avoid inhaling use only as directed intentional misuse by deliberately concentrating and inhaling the contents may be harmful or fatal Store at room temperature 59-86°F (15-30°C) do not expose to temperatures above 120°F

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-634-7680

📄 Package Label / Principal Display Panel 45 words ▾

Medi-First Blood Clotting Spray Label Medi-First® Blood Clotting Spray Aids in control of bleeding Temporarily relieves pain of minor cuts, burns and scrapes Helps prevent infection Coantains no fluorocarbons Aerosol Warning: FLAMMABLE Contents under pressure, read Back Panel Carefully Net Weight 3 oz (85g) Medi-First

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 — 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.
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 Unifirst First Aid Corporation. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Unifirst First Aid Corporation 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.
← 47682-0225-02 · Unifirst 47682-0227-12 · Unifirst →
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.