Over-the-counter drug · OTC MONOGRAPH DRUG
Hand Sanitizing Wipes NDC 57362-568
Alcohol 76 mL/100mL · Swab · Topical · Innovative Biodefense
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 57362-568-18 | 5736205681857362056818 | 5 mL in 1 PACKAGE (57362-568-18)Marketed from Aug 1, 2020 |
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)
- Hand Sanitizing Wipes
- Generic name (nonproprietary)
- hand sanitizing wipes
- Active ingredients
- Alcohol — 76 mL/100mL
- Dosage form
- Swab
- Route
- Topical
- Labeler
- Innovative BiodefenseNDC labeler code 57362
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 57362-568_05733f84-6bf7-9f6a-e063-6294a90ac5c9SPL ID 05733f84-6bf7-9f6a-e063-6294a90ac5c9SPL set ID b01d3c2c-056c-314c-e053-2a95a90a42f4RxCUI 2397694UNII 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
N457362056818followed by a unit qualifier and the quantityPackage 57362-0568-18. 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)
To decrease bacteria on skin. Recommended for repeated use.
Excerpt only. Read the full label for complete information.
About NDC 57362-568
- What is NDC 57362-568?
- 57362-568 is the product NDC for Hand Sanitizing Wipes, Alcohol 76 mL/100mL swab, listed with the FDA by Innovative Biodefense. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Hand Sanitizing Wipes.
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- Innovative Biodefense, NDC labeler code 57362. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Hand Sanitizing Wipes?
- 8 other product NDCs are listed under this name. See all Hand Sanitizing Wipes NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Hand Sanitizing Wipes products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Hand Sanitizing Wipes | Alcohol 1.69 g/2.419g | PatchTopical | SHENZHEN BENLIJU BIO-TECH CO.,LTD | 84449-007 | 84449-0007-01 |
| Hand Sanitizing Wipes | Alcohol 75 mL/100mL | ClothTopical | IMAGINE AMAZON LLC | 85380-0001 | 85380-0001-02 |
| Hand Sanitizing Wipesalcohol | Alcohol 75 mL/100mL | LiquidTopical | Germs Be Gone LLC | 84973-0075 | 84973-0075-0184973-0075-02 |
| Hand Sanitizing Wipesethyl alcohol | Alcohol 70 mL/100mL | ClothTopical | UpLift Brands LLC | 83986-028 | 83986-0028-64 |
| Hand Sanitizing Wipesethyl alcohol | Alcohol .62 mL/mL | SwabTopical | Phoenix Healthcare Solutions LLC | 60913-416 | 60913-0416-11 |
| Hand Sanitizing Wipesbenzalkonium chloride | Benzalkonium chloride 1 mg/g | ClothTopical | Ez Products Of South Florida, LLC | 69446-220 | 69446-0220-00 |
| Hand Sanitizing Wipesethyl alcohol | Alcohol .62 mL/mL | ClothTopical | PHOENIX HEALTHCARE SOLUTIONS, LLC | 60913-415 | 60913-0415-11 |
| Hand Sanitizing Wipesethyl alcohol | Alcohol 67 mL/100mL | ClothTopical | UpLift Brands, LLC | 83986-100 | 83986-0100-93 |
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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