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Clorox Healthcare GBG AloeGel ALCOHOL .71 mL/mL Cloth, 100 patches — NDC 69540-0037-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Clorox Healthcare GBG AloeGel ALCOHOL .71 mL/mL Cloth, 100 patches — NDC 69540-0037-3 (Billing 69540-0037-03)

by Brand Buzz LLC · 100 PATCH in 1 CANISTER / .71 mL in 1 PATCH

This is a package of 100 patches of Clorox Healthcare GBG AloeGel ALCOHOL .71 mL/mL Cloth from Brand Buzz LLC, no longer marketed (first marketed Aug 2021), no longer in the FDA NDC Directory.

NDC 69540-0037-03
🏷️ FDA NDC (as labeled) 69540-0037-3 billing pads the package segment with a zero
This package
Contains100 patches Pack sizes6 compare ↓
Product page 69540-0037-01 Also comes in: 20 patches 69540-0037-2 40 patches 69540-0037-5 40 packets 69540-0037-6 100 packets 69540-0037-1 270 patches 69540-0037-4
OTC Discontinued Non-controlled ⚠ Inactivated by FDA ⇄ 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 69540-0037-3 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69540 labeler · 0037 product · 3 package
Package marketed since
Oct 4, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0742797934242, 0742797934150, 0742797934136, 0742797934228 +1 more
FDA record last changed
Jul 24, 2026
⚠️
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) 69540-0037-3
Product NDC 69540-0037
11-digit billing NDC 69540003703
RxCUI 2571350
UNII 3K9958V90M
UPC 0742797934242, 0742797934150, 0742797934136, 0742797934228 +1 more
Application # M003
SPL Set ID 5dfc97d0-bc59-4377-bd79-81fa75c55618
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2021-08-24
Route TOPICAL
Dosage form CLOTH
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 2571350
Why two NDCs? The FDA registers this code as 69540-0037-3 — 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 → 69540-0037-03. 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

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 Read our full Alcohol guide →

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 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: 20 patches 40 patches 40 packets 100 packets 270 patches
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
69540-0037-01 69540-0037-1 Main listing 100 PACKET in 1 BOX / .71 mL in 1 PACKET 2021-10-04 — Inactivated by FDA
69540-0037-02 69540-0037-2 20 PATCH in 1 POUCH / .71 mL in 1 PATCH 2021-10-04 — Inactivated by FDA
69540-0037-03 You're viewing this 100 PATCH in 1 CANISTER / .71 mL in 1 PATCH 2021-10-04 — Inactivated by FDA
69540-0037-04 69540-0037-4 270 PATCH in 1 CANISTER / .71 mL in 1 PATCH 2021-10-04 — Inactivated by FDA
69540-0037-05 69540-0037-5 40 PATCH in 1 CANISTER / .71 mL in 1 PATCH 2021-10-04 — Inactivated by FDA
69540-0037-06 69540-0037-6 40 PACKET in 1 BOX / .71 mL in 1 PACKET 2021-10-04 — Inactivated by FDA

Pack size FAQ

What quantity is in this package?
This package contains 100 patches — 100 patch in 1 canister / .71 ml in 1 patch.
How does this package differ from NDC 69540-0037-02?
Both are Clorox Healthcare GBG AloeGel ALCOHOL .71 mL/mL Cloth — the drug itself is identical. This page's package is the 100 patches one, while NDC 69540-0037-02 is the 20 patches package.
What NDC number is used to bill for this package of Clorox Healthcare GBG AloeGel ALCOHOL .71 mL/mL Cloth?
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
Clorox Healthcare GBG AloeGel .71 mL/mLthis 69540-0037-03 Brand 100 patches — — Discontinued —
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
Aug 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.

🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 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 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 Y98611C087
    Glyceryl laurate is an emulsifier made by combining glycerin and lauric acid. It helps mix oil and water-based ingredients together in the medicine and may improve how the product feels or spreads.
  • UNII ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • 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 statesWater, Glycerin, Glyceral Laurate, Isopropyl Alcohol, Aloe Barbadensis Leaf Juice

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

LabelerBrand Buzz LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code69540
First marketedAug 2021
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from Brand Buzz LLC labeler code 69540

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Uses Hand sanitizing to help reduce bacteria on the skin.

⏱️ Dosage and Administration 10 words ▾

Directions Wet hands thoroughly with product and allow to dry.

⚠️ Warnings 60 words ▾

Warnings For external use only. Keep away from fire or flame. When using this product Do not use in or near the eyes. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

📦 Storage and Handling 10 words ▾

Other Information Store below 104℉ (40℃). May discolor certain fabrics.

🧪 Active Ingredient 8 words ▾

Active ingredient Ethyl Alcohol 71% v/v Purpose Antiseptic

🧪 Inactive Ingredients 11 words ▾

Ingredients Water, Glycerin, Glyceral Laurate, Isopropyl Alcohol, Aloe Barbadensis Leaf Juice

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 When Using This Product 30 words ▾

When using this product Do not use in or near the eyes. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

📄 Questions or Comments 12 words ▾

Questions of Comments? Visit us at www.brandbuzzcp.com or call us at 1-888-508-4750

📄 Package Label / Principal Display Panel 215 words ▾

CLOROX HEALTHCARE™ GBG AloeGel™ Kills 99.99% Germs* DOES NOT CONTAIN BLEACH Antibacterial Hand Wipes Clorox Healthcare™ GBG AloeGel™ Antibacterial Hand Wipes kill 99.99% of most illness causing germs, so you can confidently keep your hands clean when soap and water are not available Wipe dimensions: 5.75in. x 7.5in. (14.6 cm x 19 cm) Remove lid by lifting upward. Pull wipe from center of the roll and thread through the underside of lid.

DO NOT put finger through the hole. Close lid and pull wipe from canister at an angle. Snap lid cap shut to retain moisture.

Developed in USA | Responsibly Made in China ©2021 Distributed by Brand Buzz LLC., 1407 Broadway, New York, NY 10018 CLOROX and other trademarks are used by Brand Buzz LLC under license from The Clorox Company or its affiliates. *kills 99.99% of most illness causing germs 1x100 Wipes 20 Wipes 40 Wipes 100 Wipes 270 Wipes CLOROX™ Hand Sanitizing Wipe Kills 99.99% Germs* Alcohol-Based Bleach-Free For use on hands only 1 Wipe: 5in. x 7.5in. (12.7cm x 19cm) *kills 99.99% of most illness causing germs Dist. by: Brand Buzz LLC., 1407 Broadway, New York, NY 10018 The registered Clorox trademarks and logo are used under license by Brand Buzz LLC.

1x40 Wipes 1 1x100 20 40 100 270 1x40

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 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 5 other package presentations of this same product, including 20 patches (69540-0037-02), 40 patches (69540-0037-05), 40 packets (69540-0037-06). 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?
Brand Buzz LLC 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.
← 69540-0036-01 · Brand 69543-0107-10 · Virtus →
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.