Zep Instant Hand Sanitizer Gel Alcohol 70 mL/100mL Liquid, 15140 mL — NDC 66949-117-24 (Billing 66949-0117-24)
This is a package of 15,140 mL of Zep Instant Hand Sanitizer Gel Alcohol 70 mL/100mL Liquid from Zep Inc., marketed since Sep 2020 and currently FDA-listed.
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 3, 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 |
|---|---|---|---|---|
| 66949-0117-01 66949-117-01 Main listing | 6000 mL in 1 CASE | 2020-09-28 | — | Active |
| 66949-0117-24 You're viewing this | 15140 mL in 1 CASE | 2020-09-28 | — | Active |
| 66949-0117-32 66949-117-32 | 11400 mL in 1 CASE | 2020-09-28 | — | Active |
| 66949-0117-10 66949-117-10 | 3785 mL in 1 CASE | 2020-09-28 | — | Active |
You're viewing the largest of 4 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
How does this package differ from NDC 66949-0117-10?
What NDC number is used to bill for this package of Zep Instant Hand Sanitizer Gel Alcohol 70 mL/100mL Liquid?
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 2N8MDB79NA
A synthetic polymer used as a film-coating agent on tablets and capsules. It forms a protective barrier that controls how quickly the medicine dissolves and releases in the digestive system.
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UNII 5655G9Y8AQ
A synthetic liquid polymer used as a solvent and humectant in medications. It helps dissolve active ingredients, maintain moisture in the formulation, and improve how the medicine flows and is absorbed.
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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.
3 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 ■ To help reduce germs and bacteria on the skin. ■ Recommended for repeated use. ■ No rinsing required.
⏱️ Dosage and Administration ▾
Directions Apply gel to hands. Rub into hands for at least 20 seconds or until dry.
⚠️ Warnings ▾
Warnings Flammable. Keep away from fire, flame, or spark. For external use only.
📦 Storage and Handling ▾
Other information ■ Keep container closed and stored in a dry area at temperatures between 68°F and 77°F (20°C and 25°C). ■ Do not reuse empty container. ■ Dispose in accordance with all applicable federal, state and local regulations
🧪 Active Ingredient ▾
Active Ingredient Ethanol 70% v/v
🧪 Inactive Ingredients ▾
Inactive ingredients Deionized Water, PEG-6 (and) Acrylates/Vinyl Crosspolymer, Fragrance.
🎯 Purpose ▾
Purpose Antiseptic
📄 Do Not Use ▾
Do not use in the eye; if in eyes, rinse thoroughly with water.
📄 When Using This Product ▾
When using this product ■ Do not swallow. ■ If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask doctor Stop use and ask doctor if skin irritation or redness persists for more than 72 hours.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children and pets Keep out of reach of children and pets. Children must be supervised in use of this product.
📄 Questions or Comments ▾
Questions or comments? Call 1-877-I-BUY-ZEP (1-877-428-9937)
📄 Package Label / Principal Display Panel ▾
Package Label - Principal Display Panel 3558
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. |