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Green Guard Antideptic Wipes Benzalkonium chloride 1.3 mg/mL Swab, 25 packets — NDC 47682-0055-73 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Green Guard Antideptic Wipes Benzalkonium chloride 1.3 mg/mL Swab, 25 packets — NDC 47682-055-73 (Billing 47682-0055-73)

by Uniforst First Aid Corporation · 25 PACKET in 1 BOX / 2.1 mL in 1 PACKET

This is a package of 25 packets of Green Guard Antideptic Wipes Benzalkonium chloride 1.3 mg/mL Swab from Uniforst First Aid Corporation, marketed since Aug 2017 and currently FDA-listed. It is this product's only package size.

NDC 47682-0055-73
🏷️ FDA NDC (as labeled) 47682-055-73 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 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 47682-055-73 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
47682 labeler · 055 product · 73 package
Package marketed since
Aug 21, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 4768205573 8
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Benzalkonium Chloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 8, 2026 — CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0693-2026
Class II · Apr 8, 2026 — CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0699-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0375-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0369-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0365-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0374-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 47682-055-73
Product NDC 47682-055
11-digit billing NDC 47682005573
RxCUI 1043307
UNII F5UM2KM3W7
Application # M003
SPL Set ID 5744f9a2-35c6-37df-e053-2991aa0a1ca9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-08-21
Route TOPICAL
Dosage form SWAB
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1043307
Why two NDCs? The FDA registers this code as 47682-055-73 — 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 → 47682-0055-73. 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?

Green Guard Antideptic Wipes is a topical antiseptic swab product containing benzalkonium chloride. This active ingredient is commonly used as a broad-spectrum antimicrobial agent applied to skin to help reduce bacteria. The product is marketed as an over-the-counter monograph drug, meaning it is regulated under FDA's established rules for antiseptic wipes rather than through individual product approval. These wipes are typically used for minor skin cleansing and antiseptic purposes.

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
47682-0055-73 You're viewing this Main listing 25 PACKET in 1 BOX / 2.1 mL in 1 PACKET 2017-08-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
BZK Towelette 1.33 mg/mL 00924-7112-00 Acme 1.4 ml — — FDA listed —
First Aid Only BZK Antiseptic Towelettes 1.3 mg/mL 00924-7115-00 Acme 1.6 ml — — FDA listed —
Bzk 1.33 mg/mL 34645-5008-03 Jianerkang 1.4 ml — — FDA listed —
Medi-First Plus Antiseptic Wipes 1.3 mg/mL 47682-0030-71 Unifirst 20 packets — — FDA listed —
Green Guard Antideptic Wipes 1.3 mg/mLthis 47682-0055-73 Uniforst 25 packets — — FDA listed —
Medi-First Antiseptic Wipes 1.33 mg/mL 47682-0212-12 Unifirst 10 packets — — FDA listed —
MedPride Sterile .133 g 52410-4150-05 Shield 1000 cloths — — FDA listed —
BZK Cleansing Swabsticks 4 Triple 1.33 mg/g 59050-0263-01 Changzhou 3 packets — — FDA listed —
LIGHTS Swabstick .133 g/100g 61333-0208-01 Lights 3 applicators — — FDA listed —
CliniClean BZK Cleansing Swabsticks 1.33 mg/g 69464-0702-03 HR 6 g — — FDA listed —
Thompson Antiseptic 1.33 mg/mL 73408-0032-71 Thompson 20 packets — — FDA listed —
Thompson Antiseptic 1.3 mg/mL 73408-0034-50 Thompson 50 packets — — FDA listed —
North Woods Derma Foam Hand Sanitizer 1.3 mg/mL 53125-0700-54 Superior 1000 ml — — Discontinued —
WIPE OUT Antibacterial Wipes, Lemon Scent 1.3 mg/mL 34645-0009-01 Jianerkang 20 patches — — FDA listed —
WIPE OUT Antibacterial Wipes, Fresh Scent 1.3 mg/mL 34645-0010-01 Jianerkang 20 patches — — FDA listed —
Antibacterial FoamSoap 1.3 mg/mL 84194-0751-29 Ferguson 1000 ml — — FDA listed —
Antibacterial Hand Wipes 1.3 mg/mL 44119-0012-01 Peachtree 80 patches — — Discontinued —
Tork Hand Washing Antibacterial Foam 1.3 mg/mL 49351-0304-01 Essity 1000 ml — — FDA listed —
Pacific Blue Ultra Antimicrobial Pacific Citrus 1.3 mg/mL 54622-0712-01 Georgia-Pacific 1200 ml — — FDA listed —
Antibacterial Hand Wipes Lil Drug Store 1.3 mg/mL 66715-6863-00 Lil' 30 applicators — — FDA listed —
Dealmed BZK Antiseptic Towelettes 1.3 mg/mL 70082-0012-01 Dealmed 100 pouches — — FDA listed —
Biopure Antibacterial Hand Wipe Juicy Watermelon 1.3 mg/mL 78691-0034-00 Quest 50 ml — — FDA listed —
Antiseptic Wipe 1.3 mg/mL 83165-0002-00 Hubei 1 patch — — FDA listed —
Pacific Blue Ultra 1.3 mg/mL 54622-0572-01 Georgia-Pacific 1200 ml — — FDA listed —
Benzalkonium Chloride 1.3 mg/mL 55319-0879-03 Family 1470 ml — — FDA listed —
I.C. Waterless Hand Cleaner with Micro Scrubbers 1.3 mg/mL 59555-0303-04 R 59 ml — — FDA listed —
Antibacterial Bathing 1.3 mg/mL 63517-0210-22 Cardinal 8 patches — — FDA listed —
Germ Free Topical Antiseptic 1.3 mg/mL 71884-0008-02 Enviro 57 ml — — FDA listed —
Biopure Antibacterial Hand Wipe Berry Strawberry 1.3 mg/mL 78691-0035-00 Quest 50 ml — — FDA listed —
Transcend E2 Sanitizing Foam 1.3 mg/mL 81792-0002-01 Von 1250 ml — — FDA listed —
Foaming Hand 1.3 mg/mL 83986-0224-08 UpLift 3785 ml — — FDA listed —
HEALTH E Alcohol-Free Antiseptic 1.3 mg/mL 42326-0090-01 Petra 1000 patches — — FDA listed —
Ultra Blue Antibacterial Foaming Skin Cleanser 1.3 mg/mL 65601-0759-03 Betco 750 ml — — FDA listed —
BZK Pads 1.3 mg/mL 67777-0243-03 Dynarex 100 packets — — FDA listed —
Wipex Sanitizing Wipes 1.3 mg/mL 74680-0231-75 Unico 960 ml — — FDA listed —
Antibacterial 1.3 mg/mL 75712-0897-03 Old 1478 ml — — FDA listed —
Wipe Those Hands 1.3 mg/mL 78091-0251-02 Mighty 20 applicators — — FDA listed —
Moisturizing Antibacterial 1.3 mg/mL 79903-0164-11 Walmart 332 ml — — FDA listed —
Antibacterial Hand Wash Spring Rain 1.3 mg/mL 83986-0012-32 UpLift 355 ml — — FDA listed —
Antibacterial Hand Wash 1.3 mg/mL 83986-0015-32 UpLift 355 ml — — FDA listed —
Foaming Hand 1.3 mg/mL 11344-0224-04 Nice-Pak 750 ml — — Discontinued —
Three Cleansing 1.3 mg/mL 34645-0025-01 Jianerkang 500 pouches — — FDA listed —
enMotion Antimicrobial with Moisturizers, Tranquil Aloe 1.3 mg/mL 54622-0700-01 Georgia-Pacific 1200 ml — — FDA listed —
I.C. Antibacterial Hand Cleaner 1.3 mg/mL 59555-0701-08 R 236 ml — — FDA listed —
BZK Pads 1.3 mg/mL 67777-0245-02 Dynarex 1000 packets — — FDA listed —
Hand Wash 1.3 mg/mL 69790-0466-96 ULINE 221 ml — — FDA listed —
My-Shield Topical Antiseptic 1.3 mg/mL 71884-0025-01 Enviro 30 ml — — FDA listed —
Biopure Antibacterial Hand Wipe 1.3 mg/mL 78691-0017-00 Quest 50 patches — — Discontinued —
Club Wipes Alcohol Free Antimicrobial Cleaning Wipes 1.3 mg/mL 42326-0098-01 Petra 1200 patches — — FDA listed —
Foaming Hand 1.3 mg/mL 42961-0224-71 Cintas 800 ml — — FDA listed —
Genuine First Aid Antiseptic Towelette 1.3 mg/mL 50814-0057-01 GFA 225 ml — — FDA listed —
Hand Wash 1.3 mg/mL 71897-0466-86 Veritiv 1000 ml — — FDA listed —
OP First Aid Series Antiseptic Wipe 1.3 mg/mL 72459-0011-01 Yiwu 1 patch — — FDA listed —
Benzalkonium Chloride 1.3 mg/mL 79903-0167-50 Walmart 1470 ml — — FDA listed —
Hand Wash 1.3 mg/mL 83986-0460-04 UpLift 750 ml — — FDA listed —
Antibacterial Cherry Blossom 1.3 mg/mL 83986-0913-32 UpLift 355 ml — — FDA listed —
Antiseptic Wipe 1.3 mg/mL 34645-0024-01 Jianerkang 400 pouches — — FDA listed —
Antibacterial 1.3 mg/mL 41250-0976-68 Meijer, 1656 ml — — Discontinued —
BZK Towelette 1.3 mg/mL 65517-0004-01 Dukal 1.4 ml — — FDA listed —
Foaming Hand 1.3 mg/mL 71897-0224-86 Veritiv 1000 ml — — FDA listed —
Thompson Antiseptic 1.3 mg/mL 73408-0035-50 Thompson 50 packets — — FDA listed —
Max OUT 1.3 mg/mL 74680-0221-88 Unico 480 ml — — FDA listed —
Antibacterial Hand White Tea and Eucalyptus 1.3 mg/mL 83986-0140-32 UpLift 355 ml — — FDA listed —
White Rain Antibacterial Hand Fresh and Clean 1.3 mg/mL 52862-0627-00 International 221 ml — — Discontinued —
BZK Pads 1.3 mg/mL 67777-0244-01 Dynarex 100 packets — — FDA listed —
Doctor Inks Topical Antiseptic 1.3 mg/mL 71884-0203-01 Enviro 30 ml — — FDA listed —
Moisturizing Antibacterial 1.3 mg/mL 79903-0165-50 Walmart 1470 ml — — FDA listed —
Petra Health E Wipes Alcohol Free Antiseptic 1.3 mg/mL 42326-0100-01 Petra 1 patch — — FDA listed —
North Woods Derma Foam E-2 1.3 mg/mL 53125-0817-29 Superior 1000 ml — — FDA listed —
Biopure Antibacterial Hand Wipe Vallina Dream 1.3 mg/mL 78691-0036-00 Quest 50 ml — — FDA listed —
Moisturizing Antibacterial 1.3 mg/mL 79903-0166-50 Walmart 1470 ml — — FDA listed —
Mentholatum Moisturizing Hand Sanitizer 1.3 mg/mL 10742-0004-01 The 192 ml — — FDA listed —
Green Guard Antiseptic Wipes 1.3 mg/mL 47682-0075-73 UniFirst 25 packets — — FDA listed —
White Rain Antibacterial Hand Spring Water 1.3 mg/mL 52862-0626-00 International 221 ml — — Discontinued —
enMotion Antimicrobial with Moisturizers, Fragrance Free 1.3 mg/mL 54622-0703-01 Georgia-Pacific 1200 ml — — FDA listed —
Alcohol Free Foaming Hand Sanitizer 1.3 mg/mL 65601-0700-04 Betco 3780 ml — — FDA listed —
Zest Antibacterial Liquid Hand Soap, Fresh Aqua 1.3 mg/mL 81277-0013-01 Sodalis 221 ml — — Discontinued —
I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 1.3 mg/mL 59555-0903-03 R 50 ml — — FDA listed —
E2 Antibacterial Foaming Skin Cleanser 1.3 mg/mL 65601-0817-04 Betco 3780 ml — — FDA listed —
VLITEPRO BZK Antiseptic Towelette 1.3 mg/mL 72459-0020-01 Yiwu 1 pouch — — FDA listed —
Fresh Theory Antibacterial Hand Wipes - Peach Prosecco 1.3 mg/mL 78691-0039-00 Quest 40 ml — — FDA listed —
Fresh Theory Antibacterial Hand Wipes Fresh And Fruity 1.3 mg/mL 78691-0038-00 Quest 40 ml — — FDA listed —
Fresh Theory Antibacterial Hand Wipes - Tropical Escape 1.3 mg/mL 78691-0040-00 Quest 40 ml — — FDA listed —
FRESH THEORY ANTIBACTERIAL HAND WIPES - Vanilla, Strawberry, Fresh 1.3 mg/mL 78691-0041-01 Quest 3 canisters — — FDA listed —
B-Pure Antibacterial Wipes for Hands and Face Vitamin E and Aloe 1.3 mg/mL 80684-0233-01 Fourstar 70 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

🏛️
2017
On the market since
Aug 2017
📍
2026
Currently FDA-listed
9 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 8MDF5V39QO
    A white powder form of baking soda that acts as a buffer and pH regulator in medicines. It helps maintain the right acid-base balance and may aid tablet disintegration.
  • 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 statessodium bicarbonate, 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

LabelerUniforst First Aid Corporation
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code47682
First marketedAug 2017
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Uniforst First Aid Corporation labeler code 47682

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 📄 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 13 words ▾

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

⏱️ Dosage and Administration 25 words ▾

Directions tear open packet, unfold and clean the affected area discard after use may be covered with a sterile bandage if bandaged, let dry first

⚠️ Warnings 69 words ▾

Warnings Do not use in the eyes or applyover large area of the body in case of deep puncture wounds, animal bites or serious burns, consult a doctor longer than 1 week unless directed by a doctor Stop use and ask a doctor if the condition persists or gets worse Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 8 words ▾

Drug Facts Active ingredient Benzalkonium chloride 0.133% w/v

🧪 Inactive Ingredients 5 words ▾

Inactive ingredients sodium bicarbonate, water

🎯 Purpose 4 words ▾

Purpose First aid antiseptic

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if the condition persists or gets worse

📄 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.

📄 Other Information 20 words ▾

Other information store at room temperature 59°-86°F (15°-30°C) tamper evident sealed packets do not use any open or toen packets

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-869-6970

📄 Package Label / Principal Display Panel 77 words ▾

Green Guard Antiseptic Wipes Label Antiseptic wipes First aid to help prevent infection in minor cuts, scrapes and burns Benzalkonium chlorise 0.133% w/v First Aid Antiseptic Green Guard® 25 Extra Large Wipes Per Box Order # 3025 Green Guard Antiseptic Wipes

Green Guard Antiseptic Wipes Exra Large Label Antiseptic wipes First aid to help prevent infection in minor cuts, scrapes and burns Green Guard® 25 Extra Large Wioes Per Box Order # 3025 GG Antiseptic Label 18

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Benzalkonium chloride — the ingredient across all brands.

Top reported reactions

Drug Hypersensitivity124
Arthralgia117
Condition Aggravated115
Pain In Extremity114
Infection111
Musculoskeletal Stiffness111
Joint Swelling109

Reporter sex

0 reports

Serious outcomes

Hospitalization211
Life-threatening33
Death31
Disabling23
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 51 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 ✓ 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 Uniforst First Aid Corporation. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Uniforst 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.
← 47682-0050-22 · Unifirst 47682-0056-33 · 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.