Advanced Gel Hand Sanitizer Alcohol 70 mL/100mL Solution, 1000 mL — NDC 47593-488-26 (Billing 47593-0488-26)
This is a package of 1,000 mL of Advanced Gel Hand Sanitizer Alcohol 70 mL/100mL Solution from Ecolab Inc., no longer marketed (first marketed Nov 2012), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 6 package sizes.
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
- 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...
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per mL | Per 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. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 47593-0488-26 You're viewing this Main listing | 1000 mL in 1 POUCH | 2012-11-30 | — | Discontinued by firm |
| 47593-0488-31 47593-488-31 | 540 mL in 1 BOTTLE, PLASTIC | 2012-11-30 | Oct 31, 2027 | Active |
| 47593-0488-33 47593-488-33 | 118 mL in 1 BOTTLE, PLASTIC | 2012-11-30 | — | Discontinued by firm |
| 47593-0488-41 47593-488-41 | 750 mL in 1 BOTTLE, PLASTIC | 2012-11-30 | — | Discontinued by firm |
| 47593-0488-49 47593-488-49 | 37 mL in 1 BOTTLE, PLASTIC | 2012-11-30 | Oct 31, 2027 | Active |
| 47593-0488-56 47593-488-56 | 1200 mL in 1 BOTTLE, PLASTIC | 2012-11-30 | — | Discontinued by firm |
You're viewing one of 6 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
How does this package differ from NDC 47593-0488-49?
What NDC number is used to bill for this package of Advanced Gel Hand Sanitizer Alcohol 70 mL/100mL Solution?
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Sep 3, 2026
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.
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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.
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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.
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UNII 59TL3WG5CO
A synthetic polymer made by crosslinking acrylic acid with allyl sucrose. It thickens liquids, forms gels, and helps control how fast the medicine is released in your body.
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UNII 936JST6JCN
Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
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UNII 0THT5PCI0R
A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
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UNII XHK3U310BA
Cyclohexasiloxane is a silicon-based liquid that acts as a solvent and conditioning agent in medicines. It helps dissolve or carry other ingredients and improves how the product spreads or feels on the skin.
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UNII 4YK5Z54AT2
Denatonium benzoate is a bitter-tasting chemical compound added to medicines to discourage accidental ingestion, especially by children. It serves as a bittering agent with no therapeutic effect on the body.
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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.
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UNII Q4R969U9FR
A chelating agent derived from ethylenediamine, used in formulations to bind metal ions and prevent oxidation, helping preserve the medicine's stability and potency over time.
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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.
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UNII 8CRQ2TH63M
Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
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UNII 412ZHA4T4Y
A plant-derived oil extracted from meadowfoam seeds. It acts as an emollient and skin-conditioning agent, helping soften and smooth the product texture while improving how it spreads on skin.
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UNII WV9CM0O67Z
Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
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UNII 1212Z7S33A
PEG-32 is a synthetic polymer derived from ethylene oxide. It acts as a humectant and solvent in medications, helping to dissolve or suspend active ingredients and maintain moisture in solid dosage forms.
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UNII MD83SFE959
A volatile organic liquid used as a solvent and preservative in medications. It helps dissolve active ingredients and other components, and can improve product stability and shelf life.
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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.
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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.
17 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses For handwashing to decrease bacteria on skin
⏱️ Dosage and Administration ▾
Directions Apply product onto hands, spread thoroughly and rub until dry
⚠️ Warnings ▾
Warnings For external use only FLAMMABLE. Keep away from fire or flame, heat, sparks and sources of static discharge. Do not use In eyes When using this product If in eyes, rinse promptly and thoroughly with water Discontinue use if irritation and redness develop Stop use and ask a doctor if Skin irritation or redness occurs for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient Ethyl Alcohol 62% w/w (equivalent to 70% v/v)
🧪 Inactive Ingredients ▾
Inactive ingredients Water (Aqua), PEG-32, Cetyl Alcohol, Glycerin, Tetrahydroxypropyl Ethylenediamine, Limnanthes Alba Seed Oil , Acrylates Copolymer, Cyclopentasiloxane, Isopropyl Palmitate, Cyclohexasiloxane, t-Butyl Alcohol, Dimethicone, Tocopheryl Acetate, Titanium Dioxide, Aloe Barbadensis Leaf Juice, fragrance, Panthenol, Denatonium benzoate
🎯 Purpose ▾
Purpose Antiseptic handwash
📄 Do Not Use ▾
Do not use In eyes
📄 Ask a Doctor Before Use If ▾
Stop use and ask a doctor if Skin irritation or redness occurs for more than 72 hours
📄 When Using This Product ▾
When using this product If in eyes, rinse promptly and thoroughly with water Discontinue use if irritation and redness develop
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions? call 1.866.781.8787
📚 References ▾
Other information for additional information, see Safety Data Sheet (SDS) for emergency medical information in USA, call 1.800.328.0026
📄 Package Label / Principal Display Panel ▾
Representative label and principal display panel NDC 47593-488-41 ECOLAB Advanced Gel Hand Sanitizer CHG Compatible Active Ingredient: 62% Ethyl Alcohol w/w (equivalent to 70% v/v) 6000079 Net Contents: 25 US fl oz (750 mL) This product may be patented: www.ecolab.com/patents Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA © 2022 Ecolab USA Inc · All rights reserved Made in United States www.ecolab.com · 755159/8501/0722 SDS-WI-15014 representative label
About this NDC listing & data coverage
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. |