Over-the-counter drug · OTC MONOGRAPH DRUG
Alcare Extra Hand Sanitizer (Alcohol) NDC 11084-006
Alcohol 80 mL/100mL · Solution · Topical · SC Johnson Professional USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 11084-006-01 | 1108400060111084000601 | 47 mL in 1 BOTTLE, PLASTIC (11084-006-01)Marketed from Mar 1, 2017 | |
| 11084-006-12 | 1108400061211084000612 | 1000 mL in 1 BOTTLE, PLASTIC (11084-006-12)Marketed from Mar 1, 2017 | |
| 11084-006-13 | 1108400061311084000613 | 1 BOTTLE, PLASTIC in 1 KIT (11084-006-13) / 1000 mL in 1 BOTTLE, PLASTICMarketed from Nov 1, 2025 | |
| 11084-006-14 | 1108400061411084000614 | 2 BOTTLE, PLASTIC in 1 BOX (11084-006-14) / 1000 mL in 1 BOTTLE, PLASTICMarketed from Nov 1, 2025 | |
| 11084-006-27 | 1108400062711084000627 | 1000 mL in 1 BOTTLE, PLASTIC (11084-006-27)Marketed from Mar 1, 2017 | |
| 11084-006-40 | 1108400064011084000640 | 400 mL in 1 BOTTLE, PLASTIC (11084-006-40)Marketed from Mar 1, 2017 | |
| 11084-006-66 | 1108400066611084000666 | 1000 mL in 1 BOTTLE (11084-006-66)Marketed from Feb 17, 2023 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Alcare Extra Hand Sanitizer
- Generic name (nonproprietary)
- alcohol
- Active ingredients
- Alcohol — 80 mL/100mL
- Dosage form
- Solution
- Route
- Topical
- Labeler
- SC Johnson Professional USA, Inc.NDC labeler code 11084
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 11084-006_c6719624-10da-43d4-9ae1-eae2398d4018SPL ID c6719624-10da-43d4-9ae1-eae2398d4018SPL set ID b1c8e5d0-a766-4bf0-a385-b7b8940a0e2cRxCUI 1039339UNII 3K9958V90M
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N411084000601followed by a unit qualifier and the quantityPackage 11084-0006-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses for hand sanitizing to reduce bacteria on the skin
Excerpt only. Read the full label for complete information.
About NDC 11084-006
- What is NDC 11084-006?
- 11084-006 is the product NDC for Alcare Extra Hand Sanitizer (alcohol), Alcohol 80 mL/100mL solution, listed with the FDA by SC Johnson Professional USA, Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Alcare Extra Hand Sanitizer (Alcohol).
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- SC Johnson Professional USA, Inc., NDC labeler code 11084. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Alcare Extra Hand Sanitizer?
- 1 other product NDC are listed under this name. See all Alcare Extra Hand Sanitizer NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Alcare Extra Hand Sanitizer products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Alcare Extra Hand Sanitizeralcohol | Alcohol 85.6 mL/100mL | SolutionTopical | SC Johnson Professional USA Inc. | 11084-009 | 11084-0009-0111084-0009-1211084-0009-13+2 more |
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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