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North Woods Derma Foam Hand Sanitizer Benzalkonium Chloride 1.3 mg/mL Soap, 1000 mL — NDC 53125-0700-54 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

North Woods Derma Foam Hand Sanitizer Benzalkonium Chloride 1.3 mg/mL Soap, 1000 mL — NDC 53125-700-54 (Billing 53125-0700-54)

by Superior Chemical Corporation · 1000 mL in 1 BAG

This is a package of 1,000 mL of North Woods Derma Foam Hand Sanitizer Benzalkonium Chloride 1.3 mg/mL Soap from Superior Chemical Corporation, no longer marketed (first marketed Oct 2015), no longer in the FDA NDC Directory.

NDC 53125-0700-54
🏷️ FDA NDC (as labeled) 53125-700-54 billing pads the product segment with a zero
This package
Contains1000 mL Pack sizes4 compare ↓
Product page 53125-0700-29 Also comes in: 500 ml 53125-700-88 550 ml 53125-700-57 1000 ml 53125-700-29
OTC Discontinued Non-controlled ⚠ Inactivated by FDA ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 2, 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

⚠️
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 ↗
⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 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) 53125-700-54
Product NDC 53125-700
11-digit billing NDC 53125070054
RxCUI 1020365
UNII F5UM2KM3W7
UPC 0814410025047, 0814410022381
Application # 505G(a)(3)
SPL Set ID 861e2386-96cf-8b8e-e053-2991aa0ac57a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2015-10-01
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1020365
Why two NDCs? The FDA registers this code as 53125-700-54 — 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 → 53125-0700-54. 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?

North Woods Derma Foam Hand Sanitizer is a topical soap containing benzalkonium chloride, an antimicrobial agent. Benzalkonium chloride is typically used in hand sanitizers and topical products for its role as an antiseptic and disinfectant, intended to reduce bacteria on the skin. This is an over-the-counter product marketed under FDA's monograph rules for hand sanitizers rather than as an individually approved application.

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: 500 ml 550 ml 1000 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
53125-0700-54 You're viewing this 1000 mL in 1 BAG 2015-10-01 — Inactivated by FDA
53125-0700-57 53125-700-57 550 mL in 1 BOTTLE, PUMP 2015-10-01 — Inactivated by FDA
53125-0700-88 53125-700-88 500 mL in 1 BOTTLE, PUMP 2015-10-01 — Active
53125-0700-29 53125-700-29 Main listing 1000 mL in 1 BAG 2015-10-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1000 mL — 1000 ml in 1 bag.
How does this package differ from NDC 53125-0700-88?
Both are North Woods Derma Foam Hand Sanitizer Benzalkonium Chloride 1.3 mg/mL Soap — the drug itself is identical. This page's package is the 1000 mL one, while NDC 53125-0700-88 is the 500 ml package.
What NDC number is used to bill for this package of North Woods Derma Foam Hand Sanitizer Benzalkonium Chloride 1.3 mg/mL Soap?
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
Instant Foam Non-alcohol PURE Hand Sanitizer .13 g/100mL 11084-0300-01 SC 47 ml — — Discontinued —
Foaming Hand 1.3 mg/mL 11344-0224-04 Nice-Pak 750 ml — — Discontinued —
Benzalkonium chloride 1.3 mg/mL 11673-0681-23 Target 68 ml — — FDA listed —
QS Plus Instant Hand Sanitizer 1.3 mg/mL 13302-0457-10 Romaine 1000 ml — — Discontinued —
X3 Clean 1.3 mg/mL 26550-0001-12 X3 75 ml — — FDA listed —
Tork Hand Sanitizer Alcohol Free Foam .13 g/100mL 49351-0103-01 Essity 6 bottles — — FDA listed —
Tork Hand Sanitizing Alcohol-Free Foam 1.3 mg/mL 49351-0303-01 Essity 1000 ml — — FDA listed —
X3 Clean Foaming Hand Sanitizer 1.3 mg/mL 49354-0055-75 HK 75 ml — — FDA listed —
Ben E. Keith FIHS 1.3 mg/mL 50980-0207-12 Ben 1000 ml — — FDA listed —
American Red Cross Antiseptic Cleansing Foam .13 g/100mL 51628-4539-01 MY 177 ml — — FDA listed —
North Woods Derma Foam Hand Sanitizer 1.3 mg/mLthis 53125-0700-54 Superior 1000 ml — — Discontinued —
DermaCen Non-Alcohol Foaming Hand Sanitizer .13 g/100mL 62654-0141-14 Central 532 ml — — FDA listed —
Byotrol Hand Sanitizer 1.3 mg/mL 63002-0002-12 Advanced 1250 ml — — FDA listed —
Hand Sanitizer 1.3 g/mL 63002-0004-33 Advanced 9.76 ml — — FDA listed —
99 Plus Hand Sanitizer 1.3 mg/mL 63533-0457-10 Momar 1000 ml — — FDA listed —
Lite nFoamy Eucalyptus Mint Sanitizing Handwash 1.3 g/L 64009-0332-72 Spartan 532 l — — FDA listed —
Lite nFoamy E2 Sanitizing Handwash 1.3 g/L 64009-0333-95 Spartan 3.79 l — — FDA listed —
Enriched Foam Alcohol-Free Hand Sanitizer 13 mg/100mL 65321-0039-01 Rubbermaid 4 pouches — — FDA listed —
Alcohol Free Foaming Hand Sanitizer 1.3 mg/mL 65601-0700-04 Betco 3780 ml — — FDA listed —
Band Aid Antiseptic Cleansing 1.3 mg/mL 69968-0728-01 Kenvue 68 ml — — FDA listed —
Blue Green Foam .13 g/100mL 70411-0100-07 H2Ocean, 207 ml — — FDA listed —
ElimiShield Hunt Core Body Foam for Hunters 1.3 mg/mL 71853-0010-00 Bryson 200 ml — — FDA listed —
Germ Free 24 Hand Sanitizer 1.3 mg/mL 71884-0006-01 Enviro 50 ml — — FDA listed —
Doctor Inks Hand Sanitizer 1.3 mg/mL 71884-0201-01 Enviro 58 ml — — FDA listed —
Mountain Air Scent FOAMING HAND SANITIZER 1.3 mg/mL 74177-0040-08 K7 236 ml — — FDA listed —
Pine and Honey Scent FOAMING HAND SANITIZER 1.3 mg/mL 74177-0041-08 K7 236 ml — — FDA listed —
Simply Lavender Scent FOAMING HAND SANITIZER 1.3 mg/mL 74177-0042-08 K7 236 ml — — FDA listed —
Vanilla Coconut Scent FOAMING HAND SANITIZER 1.3 mg/mL 74177-0043-16 K7 473 ml — — FDA listed —
Foaming Hand Sanitizer 1.3 g/1000mL 75044-0280-16 American 2 bottles — — FDA listed —
American Red Cross Antiseptic Cleansing Foam .13 g/100mL 75742-0082-01 Zhejiang 177 ml — — FDA listed —
Hand Sanitizer .13 g/100mL 76370-0006-05 Tazza 1000 ml — — Discontinued —
Gentlecare Hand And Skin Sanitizer 1.3 mg/mL 78181-0020-02 PARAGON 50 ml — — FDA listed —
KleenLine Essentials Alcohol Free Foaming Hand Sanitizer 1.3 mg/mL 79258-0700-29 Brady 1000 ml — — FDA listed —
Hygiene Clean Balsam Fir Hand Sanitizer Alcohol Free 1.3 mg/mL 80499-0004-01 USA 237 ml — — FDA listed —
Hygiene Clean Leather Oak Hand Sanitizer Alcohol Free 1.3 mg/mL 80499-0005-01 USA 237 ml — — FDA listed —
Hygiene Clean Mahogany Teakwood Hand Sanitizer Alcohol Free 1.3 mg/mL 80499-0006-01 USA 237 ml — — FDA listed —
Hygiene Clean Pumpkin Spice Hand Sanitizer Alcohol Free 1.3 mg/mL 80499-0007-01 USA 237 ml — — FDA listed —
Hygiene Clean Spring Bloom Hand Sanitizer Bottle Alcohol Free 1.3 mg/mL 80499-0025-08 USA 237 ml — — FDA listed —
Hygiene Clean Lilac Garden Hand Sanitizer Bottle Alcohol Free 1.3 mg/mL 80499-0026-08 USA 237 ml — — FDA listed —
Hygiene Clean Lavender Blossom Hand Sanitizer Bottle Alcohol Free 1.3 mg/mL 80499-0027-08 USA 237 ml — — FDA listed —
Hygiene Clean Clean Cotton Hand Sanitizer 1.3 mg/mL 80499-0100-01 USA 800 ml — — FDA listed —
Hygiene Clean Eucalyptus Hand Sanitizer 1.3 mg/mL 80499-0101-01 USA 800 ml — — FDA listed —
Hygiene Clean Luxury Clean Hand Sanitizer 1.3 mg/mL 80499-0102-01 USA 800 ml — — FDA listed —
Antiseptic Foaming Hand Sanitizer 1.3 mg/mL 82442-0812-20 Target 2 bottles — — FDA listed —
NOxyDERM .13 g/100mL 83823-0001-01 NOxy 100 ml — — FDA listed —
NOxyDERM .038 g/29.5mL 83823-0002-01 NOxy 29.5 ml — — FDA listed —
Foaming Hand Sanitizer 1.3 mg/mL 83986-0118-45 UpLift 1150 ml — — FDA listed —
Guardelle .13 g/100mL 85754-0000-02 Social 52 ml — — FDA listed —
GrowDefender Antibacterial Foam 1.3 mg/mL 87109-0013-01 Grow 50.68 ml — — FDA listed —
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 —
Medi-First Plus Antiseptic Wipes 1.3 mg/mL 47682-0030-71 Unifirst 20 packets — — FDA listed —
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 —
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 —
Green Guard Antideptic Wipes 1.3 mg/mL 47682-0055-73 Uniforst 25 packets — — FDA listed —
North Woods Derma Foam E-2 1.3 mg/mL 53125-0817-29 Superior 1000 ml — — FDA listed —
Thompson Antiseptic 1.3 mg/mL 73408-0034-50 Thompson 50 packets — — 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 —
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

🏛️
2015
On the market since
Oct 2015
📍
2026
Currently FDA-listed
11 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 8J6RDU8L9X
    A synthetic green dye used to color medications. It helps make pills and capsules visually distinct so patients can easily identify their medicine.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII BYR0546TOW
    DMDM hydantoin is a preservative chemical used to prevent the growth of bacteria and fungi in medicines. It helps keep the product safe and stable throughout its shelf life.
  • UNII 603P14DHEB
    A synthetic antimicrobial chemical used as a preservative in topical and cosmetic formulations. It prevents bacterial and fungal growth in products to maintain stability and safety during storage and use.
  • UNII KTM00873VC
    A cleansing ingredient made from coconut oil and polyethylene glycol. It acts as an emulsifier and surfactant to help mix oil and water components and improve how the medicine spreads or absorbs.
  • UNII B697894SGQ
    Polyethylene glycol 400 is a clear, thick liquid made from petroleum-derived polymers. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 469OTG57A2
    Sodium pyrrolidone carboxylate is a synthetic polymer derived from pyrrolidone chemistry. It functions as a solubilizer and binder in medications, helping dissolve poorly water-soluble drugs and hold tablet ingredients together.
  • 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.

8 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive Ingredients Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

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

LabelerSuperior Chemical Corporation
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code53125
First marketedOct 2015
Product typeHuman Otc Drug
Portfolio3 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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 18 words ▾

Uses Use in a variety of public facilities. Use this product when soap and water are not available.

⏱️ Dosage and Administration 33 words ▾

Directions ​Read the entire label before using this product. ​Dispense product onto dry hands. Rub hands together until hands are dry. Use as needed between hand washes to reduce bacteria on the skin.

⚠️ Warnings 50 words ▾

Warnings For external use only. Avoid contact with eyes. Children under the age of 6 should be supervised by an adult when using this product. Discontinue use is irritation or redness develops. If irritation persists for more than 72 hours, consult a physician. KEEP OUT OF REACH OF CHILDREN .

🧪 Active Ingredient 5 words ▾

​Active Ingredient Benzalkonium Chloride 0.13%

🧪 Inactive Ingredients 19 words ▾

Inactive Ingredients Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Keep Out of Reach of Children 6 words ▾

KEEP OUT OF REACH OF CHILDREN

📄 Questions or Comments 10 words ▾

Questions or Comments? Phone: (800) 777-9343 MDS information: ​(800) 891-4965

📄 Package Label / Principal Display Panel 14 words ▾

Superior Derma Foam Hand Sanitizer 75229-00_Superior Derma Foam Hand Sanitizer. 75229 Superior Derma Foam

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 North Woods Derma Foam Hand Sanitizer (this brand).

Top reported reactions

Drug Hypersensitivity118
Condition Aggravated114
Arthralgia112
Musculoskeletal Stiffness111
Pain In Extremity111
Infection110
Hepatotoxicity108

Reporter sex

0 reports
Male · 28%
Female · 72%
Unknown · 0%

Serious outcomes

Hospitalization175
Life-threatening27
Disabling18
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 35 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 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 ✓ 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.
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 3 other package presentations of this same product, including 500 ml (53125-0700-88), 550 ml (53125-0700-57), 1000 ml (53125-0700-29). 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?
Superior Chemical 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.
← 53118-0002-01 · Precare 53125-0801-04 · Superior →
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.