Hand Sanitizer Alcohol 70 mL/100mL Gel, 750 mL — NDC 83986-456-04 (Billing 83986-0456-04)
This is a package of 750 mL of Hand Sanitizer Alcohol 70 mL/100mL Gel from UpLift Brands, LLC, marketed since Apr 2024 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.
NDC database record
One package, one record: these facts belong to NDC 83986-456-04 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 83986 labeler · 456 product · 04 package
- Package marketed since
- Apr 15, 2024
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 8398645604 8
- FDA record last changed
- Oct 1, 2026
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 3, 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 3, 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 g | 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 4, 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 |
|---|---|---|---|---|
| 83986-0456-04 You're viewing this Main listing | 750 mL in 1 BOTTLE, PLASTIC | 2024-04-15 | — | Active |
| 83986-0456-45 83986-456-45 | 1150 mL in 1 BOTTLE, PLASTIC | 2024-04-15 | — | Active |
| 83986-0456-86 83986-456-86 | 1000 mL in 1 BOTTLE, PLASTIC | 2024-04-15 | — | Active |
You're viewing the smallest of 3 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
How does this package differ from NDC 83986-0456-86?
What NDC number is used to bill for this package of Hand Sanitizer Alcohol 70 mL/100mL Gel?
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 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.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
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.
-
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 G7515SW10N
A waxy liquid derived from vegetable oil and fatty acids. It works as an emulsifier and solubilizer to help blend oil and water-based ingredients together and improve how the medicine dissolves and is absorbed in the body.
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UNII 0RE8K4LNJS
Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
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UNII HNV0L650LG
A mild cleansing agent derived from meadowfoam plant oil. In medicines, it works as a surfactant to help mix oil and water components and improve how the product spreads on skin or is absorbed.
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UNII GIA7T764OD
A silicone-based ingredient combined with polyethylene glycol. It acts as an emulsifier and surfactant to help blend oils and water-based ingredients, and reduces foaming in liquid formulations.
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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 3, 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
More NDCs from UpLift Brands, LLC labeler code 83986
- Citroma Magnesium Citrate 1.745 g/29.6mL Liquid NDC 83986-166-38
- Hand Sanitizer Alcohol 62 mL/100mL Spray NDC 83986-199-14
- Foaming Hand Benzalkonium Chloride 1.3 mg/mL Soap NDC 83986-224-08
- Moisturizing Antibacterial Benzalkonium chloride 0.13% 1.3 mg/mL Soap NDC 83986-279-08
- Advanced Hand Sanitizer Ethyl Alcohol 70 mL/100mL Gel NDC 83986-439-16
- Moisturizing Hand Sanitizer Ethyl Alcohol 62 mL/100mL Gel NDC 83986-447-45
- Hand Wash Benzalkonium chloride 1.3 mg/mL Soap NDC 83986-460-04
- Ethyl Alcohol 62 mL/100mL Liquid NDC 83986-471-16
- Hand Sanitizer Ethyl alcohol 70 mL/100mL Gel NDC 83986-529-16
- Hand Sanitizer Alcohol 62 mL/100mL Gel NDC 83986-652-04
- Hand Sanitizer Ethyl Alcohol .62 mL/mL Spray NDC 83986-721-20
- 70% Isopropyl Alcohol 70 mL/100mL Liquid NDC 83986-810-17
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 ▾
Use to decrease bacteria on the skin that could cause disease recommended for repeated use
⏱️ Dosage and Administration ▾
Directions wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult suervision not recommended for infants
⚠️ Warnings ▾
Warnings For external use only: hands Flammable. Keep away from fire or flame.
🤒 Adverse Reactions ▾
Adverse reaction DSP-TN-21091 DSP-MO-20087 Pat. 9,161,982 DISTRIBUTED BY: UPLIFT BRANDS, LLC ST. LOUIS, MO 63114 1-866 MY GERMX
📦 Storage and Handling ▾
Other information do not store above 105° F may discolor some fabrics harmful to wood finishes and plastics
🧪 Active Ingredient ▾
Active ingredient Ethyl alcohol 70%
🧪 Inactive Ingredients ▾
Inactive ingredients water, PEG-8 Dimethicone, meadowfoamamidopropyl betaine, glyceryl caprylate/caprate, glycerin, tocopheryl acetate, isopropyl myristate
🎯 Purpose ▾
Purpose Antiseptic
📄 When Using This Product ▾
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin do not inhale or ingest
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if irritation or redness develops condition persists for more than 72 hours
📄 Keep Out of Reach of Children ▾
Keep out of reach children If swallowed, get medical help or contact a Poison Control Center right away.
📄 Package Label / Principal Display Panel ▾
Principal display panel germ-x ® PRO ADVANCED FOAMING HAND SANITIZER 1000 mL (1.05 QT)
33.8 FL OZ image description image description
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. |