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Mentholatum Moisturizing Hand Sanitizer benzalkonium chloride 1.3 mg/mL Gel, 192 mL — NDC 10742-0004-01 package photo

Mentholatum Moisturizing Hand Sanitizer benzalkonium chloride 1.3 mg/mL Gel, 192 mL

by The Mentholatum Company · 192 mL in 1 BOTTLE (10742-0004-1)
NDC 10742-0004-01
🏷️ FDA NDC (as labeled) 10742-0004-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

⚠️
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-0360-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 10742-0004-1
Product NDC 10742-0004
11-digit billing NDC 10742000401
RxCUI 1098199
UNII F5UM2KM3W7
Application # M003
SPL Set ID 365c93bc-2299-4e69-ba3a-69414bfe78d7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-06-12
Route TOPICAL
Dosage form GEL
Substance BENZALKONIUM CHLORIDE
GCN Seq No 005884
GCN 23010
HICL code 002512
Ingredient (HICL) Aminobenzoic Acid
HIC1 code L
Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue
HIC2 code L5
Therapeutic class — intermediate (HIC2) Keratolytics/Keratoplastics
HIC3 code L5B
Therapeutic class — specific (HIC3) Sunscreens
AHFS code 84:80.00.00
AHFS class Sunscreen Agents
FDB label name MENTHOLATUM LIPBALM STICK
FDB brand name Mentholatum Lipbalm
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 10742-0004-1 — a 5-4-1 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 package segment → 10742-0004-01. 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.

🏭 Manufacturer & labeler

LabelerThe Mentholatum Company
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code10742
First marketedJun 2020
Product typeHuman Otc Drug
Portfolio108 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.

🩺 Clinical

Label name MENTHOLATUM LIPBALM STICK Ingredient Aminobenzoic Acid
🧪 What is this product?

Mentholatum Moisturizing Hand Sanitizer is a topical gel marketed as an over-the-counter product under FDA's OTC monograph rules. The active ingredient benzalkonium chloride is an antimicrobial agent typically used in hand sanitizers and topical antiseptic products to reduce bacteria on the skin. This product is intended for hand hygiene use as an alternative to soap and water.

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.

🧪 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 I670DAL4SZ
    A preservative that fights bacteria and fungi. It keeps medicines and topical products stable and safe from microbial contamination during storage and use.
  • 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 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • UNII 9F8ET54T05
    A modified starch derived from high-amylose corn that has been chemically treated with propylene oxide and phosphate groups. It acts as a binder and disintegrant in tablets and capsules, helping the medicine hold together while also breaking apart in the stomach for absorption.
  • UNII 76LN7P7UCU
    Lauryl glucoside is a mild plant-based cleansing agent made from coconut oil and glucose. It's used in medicines as a surfactant to help dissolve and distribute ingredients evenly throughout the formulation.
  • UNII J3QD0LD11P
    A synthetic compound made by combining glucose with methyl alcohol and polyethylene glycol. It acts as an emulsifier and solvent to help blend water and oil-based ingredients and improve how the medicine dissolves or spreads.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 0L414VCS5Y
    A synthetic polymer used as a film-former and conditioning agent. It helps create a protective coating on hair or skin surfaces and improves texture and manageability in topical formulations.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII E52D0J3TS5
    Silanetriol is a silicon-based chemical compound used in medicines as a glidant and anti-caking agent. It helps powders flow smoothly during manufacturing and prevents clumping in the final product.
  • 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.

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

The official label also statespurified water, hydroxypropyl starch phosphate, lauryl glucoside, dimethicone, chlorphenesin, edetate disodium, glycerin, hyaluronic acid, methyl gluceth-20, phenoxyethanol, polyquaternium-7, rosmarinus officinalis (rosemary) leaf oil, silanetriol

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.

💲 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 gPer 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Mentholatum Moisturizing Hand Sanitizer 1.3 mg/mLthis 10742-0004-01 The 192 ml — — FDA listed —
XtraCare Foaming Hand Sanitizer 3 g/207g 57337-0057-01 Rejoice 207 g — — FDA listed —
Germ Free Topical Antiseptic 1.3 mg/mL 71884-0008-02 Enviro 57 ml — — FDA listed —
My-Shield Hand Sanitizer Gel .13 g/100mL 71884-0011-01 Enviro 3 tubes — — Discontinued —
My-Shield Topical Antiseptic 1.3 mg/mL 71884-0025-01 Enviro 30 ml — — FDA listed —
Doctor Inks Topical Antiseptic 1.3 mg/mL 71884-0203-01 Enviro 30 ml — — FDA listed —
NasalGuard Antiseptic Topical Cool Menthol 1.3 mg/1000mg 81907-0101-03 TRUTEK 1 tube — — FDA listed —
Unscented NasalGuard Antiseptic Topical 1.3 mg/1000mg 81907-0102-03 TRUTEK 1 tube — — 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 —
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 —
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 —
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 —
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 —
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 —
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

🏛️
2020
On the market since
Jun 2020
📍
2026
Currently FDA-listed
6 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
10742-0004-01 You're viewing this 192 mL in 1 BOTTLE (10742-0004-1) 2020-06-12 Active

🧭 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 FDA registers it as 10742-0004-1, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 10742-0004-01, written without dashes as 10742000401. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 10742-0004-01, the first segment (10742) is the labeler code FDA assigned to The Mentholatum Company; the middle segment (0004) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
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 The Mentholatum Company. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
The Mentholatum Company 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.

📄 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
🎯 Indications and Usage 9 words ▾

Uses Hand sanitizer to reduce bacteria on the skin

⏱️ Dosage and Administration 31 words ▾

Directions Liberally apply product in your palm to thoroughly cover your hands Rub hands together briskly until absorbed. Children under 6 years of age should be supervised when using this product.

⚠️ Warnings 45 words ▾

Warnings For external use only When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children.

🧪 Active Ingredient 5 words ▾

Active ingredients Benzalkonium Chloride 0.13%

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients purified water, hydroxypropyl starch phosphate, lauryl glucoside, dimethicone, chlorphenesin, edetate disodium, glycerin, hyaluronic acid, methyl gluceth-20, phenoxyethanol, polyquaternium-7, rosmarinus officinalis (rosemary) leaf oil, silanetriol

🎯 Purpose 3 words ▾

Purpose Skin antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 10742-0002-01 · The 10742-0009-01 · The →
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.