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bolor sanitizing hand wipes 12 mg/100mg Solution — NDC 77665-0001-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

bolor sanitizing hand wipes 12 mg/100mg Solution — NDC 77665-001-02 (Billing 77665-0001-02)

by Guangzhou Baihua Co., Ltd · 60 PACKET in 1 PACKET / 100 mg in 1 PACKET

This is a package of bolor sanitizing hand wipes 12 mg/100mg Solution from Guangzhou Baihua Co., Ltd, marketed since Apr 2025 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 77665-0001-02
🏷️ FDA NDC (as labeled) 77665-001-02 billing pads the product segment with a zero
This package
Contains100 mg in 1 packet Pack sizes3 compare ↓
Main listing for product 77665-001 · Also comes in: 10 packets 77665-001-06 30 packets 77665-001-04
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

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

NDC database record

One package, one record: these facts belong to NDC 77665-001-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
77665 labeler · 001 product · 02 package
Package marketed since
Apr 1, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7766500102 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 77665-001-02
Product NDC 77665-001
11-digit billing NDC 77665000102
UNII F5UM2KM3W7
SPL Set ID 33dbe9e3-4335-ada1-e063-6294a90ad2f5
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-04-01
Route TOPICAL
Dosage form SOLUTION
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 77665-001-02 — 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 → 77665-0001-02. 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.

Clinical

🧪 What is this product?

Bolor Sanitizing Hand Wipes is a topical solution containing benzalkonium chloride, an antimicrobial agent typically used in hand sanitizers and antiseptic products to reduce bacteria and other microorganisms on the skin. This product is an unapproved drug and has not received FDA marketing approval. The wipes are designed for external application to the hands as a sanitizing product.

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 mLPer 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: 10 packets 30 packets
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
77665-0001-02 You're viewing this Main listing 60 PACKET in 1 PACKET / 100 mg in 1 PACKET 2025-04-01 — Active
77665-0001-04 77665-001-04 30 PACKET in 1 PACKET / 100 mg in 1 PACKET 2025-04-01 — Active
77665-0001-06 77665-001-06 10 PACKET in 1 PACKET / 100 mg in 1 PACKET 2025-04-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 60 packet in 1 packet / 100 mg in 1 packet.
What NDC number is used to bill for this package of bolor sanitizing hand wipes 12 mg/100mg Solution?
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
bolor sanitizing hand wipes 12 mg/100mg 85577-0001-02 EcoRhine 60 packets — — FDA listed —
bolor sanitizing hand wipes 12 mg/100mgthis 77665-0001-02 Guangzhou 60 packets — — 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

🏛️
2025
On the market since
Apr 2025
📍
2026
Currently FDA-listed
1 year 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 RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII 7M867G6T1U
    Centella asiatica is a plant extract used in medicines as a skin-conditioning or soothing ingredient. It helps maintain product stability and may support skin comfort in topical formulations.
  • UNII 3L7GR2604E
    A synthetic compound derived from glycerol and formaldehyde, used as a solvent and humectant in liquid formulations to help dissolve active ingredients and maintain moisture content in the product.
  • UNII 1X0T378SXY
    An extract from honeysuckle plant flowers used as a natural flavoring and botanical ingredient. It adds taste and aroma to the medicine.
  • 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.

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

The official label also statesInactive ingredients Aloe Barbadensis Leaf Extract, Centella AsiaƟca Extract, Chlorhexidine Diacetate, Deionized Water, Ethylhexylglycerin, Glycerol, Lonicera Caprifolium Extract.

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

LabelerGuangzhou Baihua Co., Ltd
Labeler code77665
First marketedApr 2025
Product typeHuman Otc Drug
Portfolio9 products on file

More NDCs from Guangzhou Baihua Co., Ltd labeler code 77665

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 16 words ▾

When using this product avoid contact with eyes. In case of contact, flush eyes with water

⏱️ Dosage and Administration 31 words ▾

Directions Take wipe and rub thoroughly over all surfaces of both hands. Wet hands thoroughly with wipe. Rub hands together briskly to dry your hands. Dispose of wipe. Do not flush.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 7 words ▾

Active ingredient Purpose Benzalkonium chloride 0.12% Antimicrobial

🧪 Inactive Ingredients 18 words ▾

Inactive ingredients Aloe Barbadensis Leaf Extract, Centella AsiaƟca Extract, Chlorhexidine Diacetate, Deionized Water, Ethylhexylglycerin, Glycerol, Lonicera Caprifolium Extract.

🎯 Purpose 2 words ▾

Purpose Antimicrobial

📄 Keep Out of Reach of Children 31 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Children under 6 years age should be supervised when using this product.

📄 Package Label / Principal Display Panel 149 words ▾

Drug Facts Active ingredient Purpose Benzalkonium chloride 0.12% Antimicrobial Uses Hand sanitizer to help reduce bacteria on skin Recommended for repeated use When using this product avoid contact with eyes. In case of contact, flush eyes with water. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. Children under 6 years age should be supervised when using this product. Stop use and ask a doctor if irritation and/or rash occurs and persists for more than 72 hours.

Warnings For external use only Directions Take wipe and rub thoroughly over all surfaces of both hands. Wet hands thoroughly with wipe. Rub hands together briskly to dry your hands.

Dispose of wipe. Do not flush. Inactive ingredients Aloe Barbadensis Leaf Extract, Centella AsiaƟca Extract, Chlorhexidine Diacetate, Deionized Water, Ethylhexylglycerin, Glycerol, Lonicera Caprifolium Extract.

60 Packets 30 Packets Box for Box Packing

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 Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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 "Unapproved Drug Other". 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 Guangzhou Baihua Co., Ltd. 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 10 packets (77665-0001-06), 30 packets (77665-0001-04). 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?
Guangzhou Baihua 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.
← 77658-0001-01 · JUDITH 77665-0002-02 · Guangzhou →
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.