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Vaseline Clinical Care Hand Sanitizer Lotion 1.3 mg/mL Lotion, 88.5 mL — NDC 64942-1849-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Vaseline Clinical Care Hand Sanitizer Lotion 1.3 mg/mL Lotion, 88.5 mL — NDC 64942-1849-1 (Billing 64942-1849-01)

by Conopco Inc. d/b/a/ Unilever · 88.5 mL in 1 TUBE

This is a package of 88.5 mL of Vaseline Clinical Care Hand Sanitizer Lotion 1.3 mg/mL Lotion from Conopco Inc. d/b/a/ Unilever, marketed since Jan 2021 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 64942-1849-01
🏷️ FDA NDC (as labeled) 64942-1849-1 billing pads the package segment with a zero
This package
Contains88.5 mL Pack sizes3 compare ↓
Main listing for product 64942-1849 · Also comes in: 150 ml 64942-1849-2 236 ml 64942-1849-4
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 64942-1849-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
64942 labeler · 1849 product · 1 package
Package marketed since
Jan 29, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6494218491 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 64942-1849-1
Product NDC 64942-1849
11-digit billing NDC 64942184901
RxCUI 1046442
UNII F5UM2KM3W7
Application # M016
SPL Set ID ba0aa323-8887-597f-e053-2995a90a2077
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-01-29
Route TOPICAL
Dosage form LOTION
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1046442
Why two NDCs? The FDA registers this code as 64942-1849-1 — 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 → 64942-1849-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

Vaseline Clinical Care Hand Sanitizer Lotion is a topical lotion containing benzalkonium chloride, an antimicrobial agent commonly used in over-the-counter hand sanitizer and skin antiseptic products. This product is marketed under the FDA's OTC monograph rules for hand sanitizers rather than as an individually reviewed drug application. Benzalkonium chloride functions as an antimicrobial ingredient typically found in products intended to reduce bacteria on the skin.

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 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.
Try another pack size: 150 ml 236 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
64942-1849-01 You're viewing this Main listing 88.5 mL in 1 TUBE 2021-01-29 — Active
64942-1849-02 64942-1849-2 150 mL in 1 TUBE 2021-01-29 — Active
64942-1849-04 64942-1849-4 236 mL in 1 BOTTLE, PUMP 2021-01-29 — Active

Pack size FAQ

What quantity is in this package?
This package contains 88.5 mL — 88.5 ml in 1 tube.
How does this package differ from NDC 64942-1849-02?
Both are Vaseline Clinical Care Hand Sanitizer Lotion 1.3 mg/mL Lotion — the drug itself is identical. This page's package is the 88.5 mL one, while NDC 64942-1849-02 is the 150 ml package.
What NDC number is used to bill for this package of Vaseline Clinical Care Hand Sanitizer Lotion 1.3 mg/mL Lotion?
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
Target Up and Up 2-in-1 Hand Sanitizer 1.3 mg/mL 11673-0147-15 TARGET 150 ml — — FDA listed —
Zylast Antiseptic K .13 g/100mL 57362-0468-00 Innovative 59.1 ml — — FDA listed —
I.C. Waterless Hand Cleaner with Micro Scrubbers 1.3 mg/mL 59555-0303-04 R 59 ml — — FDA listed —
I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 1.3 mg/mL 59555-0903-03 R 50 ml — — FDA listed —
Vaseline 1.3 mg/mLthis 64942-1849-01 Conopco 88.5 ml — — FDA listed —
Dr Lift Antibacterial .156 mg/120mg 68062-2243-01 Spa 120 mg — — FDA listed —
Dermadive Ultracare - Tetraid .13 g/100mL 78663-0102-34 Releaf 100 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

🏛️
2021
On the market since
Jan 2021
📍
2026
Currently FDA-listed
5 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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII P01OUT964K
    A fragrant plant-derived alcohol used as a flavoring agent and fragrance component in medicines. It provides taste and aroma to make the product more pleasant to use.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 609A3V1SUA
    A silky liquid derived from caprylic acid that acts as an emollient and solvent in formulations. It helps dissolve active ingredients and improves the spreadability and feel of lotions, creams, and topical products.
  • 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 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 GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • 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 41QWS48DFN
    A synthetic polymer used as a thickening agent and film-former in topical medicines. It increases product viscosity, helps medications spread evenly on skin, and improves how long the product stays in place.
  • UNII 24SC3U704I
    A powdery carbohydrate extracted from tapioca plant roots. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your digestive system.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • 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 statesWater (Aqua), Glycerin, Tapioca Starch, Polyquaternium-37, Dicaprylyl Carbonate, Phenoxyethanol, Caprylyl Glycol, Fragrance (Parfum), Lauryl Glucoside, Tocopheryl Acetate, Citronellol, Limonene, Linalool, Titanium Dioxide (CI 77891)

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

LabelerConopco Inc. d/b/a/ Unilever
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code64942
First marketedJan 2021
Product typeHuman Otc Drug
Portfolio360 products on file

More NDCs from Conopco Inc. d/b/a/ Unilever labeler code 64942

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 📋 Description 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 7 words ▾

Uses helps decrease bacteria on the hands

⏱️ Dosage and Administration 22 words ▾

Directions Apply product thoroughly to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed.

⚠️ Warnings 29 words ▾

Warnings For external use only Avoid contact with eyes, In case of contact, rinse eyes thoroughly with water. If irritation develops, discontinue use and consult a doctor . .

🧪 Active Ingredient 7 words ▾

Drug Facts Active ingredient Benzalkonium Chloride 0.13%

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients Water (Aqua), Glycerin, Tapioca Starch, Polyquaternium-37, Dicaprylyl Carbonate, Phenoxyethanol, Caprylyl Glycol, Fragrance (Parfum), Lauryl Glucoside, Tocopheryl Acetate, Citronellol, Limonene, Linalool, Titanium Dioxide (CI 77891)

🎯 Purpose 2 words ▾

Purpose Antibacterial

📋 Description 16 words ▾

VASELINE CLINICAL CARE HAND SANITIZER LOTION - Benzalkonium Chloride lotion Vaseline Clinical Care Hand Sanitizer Lotion

📄 Keep Out of Reach of Children 24 words ▾

• Keep out of reach of children except under adult supervision. If swallowed, get medical help or contact a poison control Center right away.

📄 Questions or Comments 4 words ▾

Questions or Comments? 1-800-457-7964

📄 Package Label / Principal Display Panel 5 words ▾

Packaging Vaseline Hand Sanitizer Lotion

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 ✓ 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 Conopco Inc. d/b/a/ Unilever. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 150 ml (64942-1849-02), 236 ml (64942-1849-04). 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?
Conopco Inc. d/b/a/ Unilever 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.
← 64942-1848-01 · Conopco 64942-1853-01 · Conopco →
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.