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Strawberry Shortcake Strawberry Hand Sanitizer Wipes HAND SANITIZING 13 mg/10mL Cloth — NDC 85844-0510-02 package photo

Strawberry Shortcake Strawberry Hand Sanitizer Wipes HAND SANITIZING 13 mg/10mL Cloth

by Zhejiang Bright Care Co., Ltd · 20 PATCH in 1 CANISTER (85844-510-02) / 25 mL in 1 PATCH (85844-510-01)
NDC 85844-0510-02
🏷️ FDA NDC (as labeled) 85844-510-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 10, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

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

🆔 Identity & classification

FDA NDC (as labeled) 85844-510-02
Product NDC 85844-510
11-digit billing NDC 85844051002
RxCUI 1038558
UNII F5UM2KM3W7
Application # M003
SPL Set ID 598e08a1-3f78-47fe-e063-6394a90a645b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-06-01
Route TOPICAL
Dosage form CLOTH
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 85844-510-02 — 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 → 85844-0510-02. 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

LabelerZhejiang Bright Care Co., Ltd
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code85844
First marketedJun 2026
Product typeHuman Otc Drug
Portfolio14 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

🧪 What is this product?

This product is a hand sanitizing wipe cloth containing benzalkonium chloride, an antimicrobial agent typically used to reduce bacteria and other germs on the skin. The wipes are applied topically to the hands and are marketed as an over-the-counter hand sanitizer under the FDA's OTC monograph rules for antiseptic products. Benzalkonium chloride is a common active ingredient in hand sanitizers and other topical antimicrobial products intended for general hygiene purposes.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • 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.
  • UNII 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • 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.

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

The official label also statesAqua,Phenoxyethano,Aloe Barbadensis Extrac,Parfum

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Vanill Hand Sanitizing Wipes 13 mg/10mL 85844-0500-02 Zhejiang 20 patches — — FDA listed —
Wild Cherry Hand Sanitizing Wipes 13 mg/10mL 85844-0501-02 Zhejiang 20 patches — — FDA listed —
Mistify Vanilla Cupcake Hand Sanitizing Wipes 13 mg/10mL 85844-0515-02 Zhejiang 20 patches — — FDA listed —
Baja Blast Hand Sanitizing Wipes 13 mg/10mL 85844-0503-02 Zhejiang 20 patches — — FDA listed —
Mistify Sweet Strawberry Hand Sanitizing Wipes 13 mg/10mL 85844-0512-02 Zhejiang 20 patches — — FDA listed —
Moutain Dew Hand Sanitizing Wipes 13 mg/10mL 85844-0504-02 Zhejiang 20 patches — — FDA listed —
Mistify Sea Salt Caramel Hand Sanitizing Wipes 13 mg/10mL 85844-0514-02 Zhejiang 20 patches — — FDA listed —
Mistify Cherry Crush Hand Sanitizing Wipes 13 mg/10mL 85844-0513-02 Zhejiang 20 patches — — FDA listed —
Mistify Sweet Strawberry Hand Sanitizing Wipes 13 mg/10mL 73928-0601-02 KING 20 patches — — FDA listed —
Sherk Watermelon Hand Sanitizer Wipes 13 mg/10mL 85844-0520-02 Zhejiang 20 patches — — FDA listed —
Shrek Waffle And Ssyrup Hand Sanitizing Wipes 13 mg/10mL 85844-0522-02 Zhejiang 20 patches — — FDA listed —
Shrek Green Apple Hand Sanitizing Wipes 13 mg/10mL 85844-0523-02 Zhejiang 20 patches — — FDA listed —
Strawberry Shortcake Raspberry Hand Sanitizer Wipes 13 mg/10mL 85844-0508-02 Zhejiang 20 patches — — FDA listed —
Strawberry Shortcake Strawberry Hand Sanitizer Wipes 13 mg/10mLthis 85844-0510-02 Zhejiang 20 patches — — FDA listed —
Strawberry Shortcake Berry Twist Hand Sanitizer Wipes 13 mg/10mL 85844-0509-02 Zhejiang 20 patches — — 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

🏛️
2026
On the market since
Jun 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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
85844-0510-02 You're viewing this 20 PATCH in 1 CANISTER (85844-510-02) / 25 mL in 1 PATCH (85844-510-01) 2026-06-01 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 85844-510-02, 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: 85844-0510-02, written without dashes as 85844051002. 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 85844-0510-02, the first segment (85844) is the labeler code FDA assigned to Zhejiang Bright Care Co., Ltd; the middle segment (0510) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Zhejiang Bright Care Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Zhejiang Bright Care Co., Ltd 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 10 words ▾

To decrease bacteria on the skin Recommended for repeated use

⏱️ Dosage and Administration 18 words ▾

Wipe hands, skin surface thoroughly; Allow to dry. Use as needed for skin disinfection. For external use only.

⚠️ Warnings 61 words ▾

For external use only. When using this product key away from eye In case of eye contact, rinse eyes with doctor. Stop use and ask a doctor if: irritation and redness develop. If condition persists for more than 72 hours consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Centre right away

🧪 Active Ingredient 4 words ▾

Benzalkonium chloride 0.13% Antiseptic

🧪 Inactive Ingredients 3 words ▾

Aqua,Phenoxyethano,Aloe Barbadensis Extrac,Parfum

🎯 Purpose 1 words ▾

Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85844-0509-02 · Zhejiang 85844-0512-02 · Zhejiang →
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.