Kay Alcohol Foam Hand Sanitizer 70 mL/100mL Solution, 1200 mL — NDC 47593-686-56 (Billing 47593-0686-56)
This is a package of 1,200 mL of Kay Alcohol Foam Hand Sanitizer 70 mL/100mL Solution from Ecolab Inc., marketed since Dec 2025 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 47593-686-56 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 47593 labeler · 686 product · 56 package
- Package marketed since
- Dec 31, 2025
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 4759368656 4
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 616805
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
RxNorm drug class
This medicine belongs to the Other antiseptics and disinfectants class.
Where does this data come from?
- RxClass (NLM) · catalog 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 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 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 8, 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 |
|---|---|---|---|---|
| 47593-0686-56 You're viewing this Main listing | 1200 mL in 1 BOTTLE | 2025-12-31 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 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 Oct 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.
🧪 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.
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UNII 36HQN158VC
Alpha-bisabolol is a naturally derived oily liquid from plant sources. It works as a fragrance, flavor, and skin-conditioning agent in topical medicines and cosmetic products.
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UNII 2CNS542YRT
A silicone-based compound that acts as an emulsifier and surfactant to help blend oil and water ingredients together. It improves the texture and spreadability of topical products like creams and lotions.
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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 147D247K3P
Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
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UNII EB41QIU6JL
Farnesol is a natural fragrant compound found in plants. It's used in medicines as a preservative and flavoring agent to improve taste and help prevent microbial growth.
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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 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.
7 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 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 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
More NDCs from Ecolab Inc. labeler code 47593
- SSDC Alphasan Hand Sanitizer Alcohol 60 mL/100mL Solution NDC 47593-680-25
- MYSTIC FOAMING ANTI-BACTERIAL HANDSOAP Benzalkonium Chloride 5 mg/mL Solution NDC 47593-681-41
- RUSHING FOAMING ANTIBACTERIAL HANDSOAP Chloroxylenol 5 mg/mL Solution NDC 47593-682-59
- Kay Hand Sanitizer Foam Ethyl Alcohol 54.7 g/100g Solution NDC 47593-683-96
- Retail Hand Sanitizer Alcohol 60 mL/100mL Liquid NDC 47593-684-56
- Ecolab Retail Foaming Alcohol Hand Sanitizer 70 mL/100mL Solution NDC 47593-685-56
- CHEMSTAR RETAIL HAND SANITIZER Alcohol 60 mL/100mL Liquid NDC 47593-687-56
- CHEMSTAR Chloroxylenol .5 mg/100mL Solution NDC 47593-688-59
- CHEMSTAR Foaming Hand Sanitizer Benzalkonium chloride .1 mg/100mL Solution NDC 47593-689-59
- Alcohol Gel Hand Sanitizer 60 mL/100mL Solution NDC 47593-690-70
- EXP Foaming Hand Sanitizer Benzalkonium chloride .1 mg/100mL Solution NDC 47593-692-70
- Kay RTU Foaming AB HandSoap Chloroxylenol 5 mg/mL Solution NDC 47593-693-70
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses for hand washing to decrease bacteria on the skin
⏱️ Dosage and Administration ▾
Directions wash hands to remove soil spread to cover hands thoroughly, rub to 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 throughly with water discontinue use if irritation and redness develop Stop use and ask doctor if skin irritation and redness persists from 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-10 dimethicone, ethylhexylglycerin, farnesol, bisabolol, tert-butyl alcohol, denatonium benzoate
🎯 Purpose ▾
Purpose Antiseptic handwash
📄 Do Not Use ▾
Do not use in eyes
📄 Ask a Doctor Before Use If ▾
Stop use and ask doctor if skin irritation and redness persists from more than 72 hours
📄 When Using This Product ▾
When using this product if in eyes, rinse promptly and throughly 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 1-800-529-5458
📚 References ▾
Other information for additional information, see Safety Data Sheet (SDS) for emergency medical information in USA, call (877) 231-2615 or call collect - 0 (952) 853-1713
📄 Package Label / Principal Display Panel ▾
Principal display panel and representative label KAY Alcohol Foam Hand Sanitizer Active ingredient: Ethyl alcohol 62% w/w (equivalent to 70% v/v) Net contents:
40.6US fl oz (1200 mL) SDS-NC-872, SDS-WI-15014, SDS-NJ-20007 Distributed by Kay Chemical Company 8300 Capital Drive - Greensboro NC 27409-9790 USA Customer Service: (800) 529-5458 (c)2020 Kay Chemical Company All rights reserved Made in USA 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. |