Over-the-counter drug · OTC MONOGRAPH DRUG
Purell Advanced Soothing (Alcohol) NDC 21749-713
Alcohol .7 mL/mL · Gel · Topical · GOJO Industries, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 21749-713-02 | 2174907130221749071302 | 59 mL in 1 BOTTLE (21749-713-02)Marketed from Nov 1, 2018 | |
| 21749-713-04 | 2174907130421749071304 | 118 mL in 1 PACKAGE (21749-713-04)Marketed from Nov 1, 2018 | |
| 21749-713-08 | 2174907130821749071308 | 236 mL in 1 BOTTLE (21749-713-08)Marketed from Nov 1, 2018 | |
| 21749-713-10 | 2174907131021749071310 | 295 mL in 1 PACKAGE (21749-713-10)Marketed from Nov 1, 2018 | |
| 21749-713-12 | 2174907131221749071312 | 354 mL in 1 BOTTLE (21749-713-12)Marketed from Nov 1, 2018 | |
| 21749-713-24 | 2174907132421749071324 | 710 mL in 1 PACKAGE (21749-713-24)Marketed from Aug 1, 2021 | |
| 21749-713-33 | 2174907133321749071333 | 1000 mL in 1 PACKAGE (21749-713-33)Marketed from Nov 1, 2018 | |
| 21749-713-65 | 2174907136521749071365 | 192 mL in 1 PACKAGE (21749-713-65)Marketed from Jul 1, 2021 |
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)
- Purell Advanced Soothing
- Generic name (nonproprietary)
- alcohol
- Active ingredients
- Alcohol — .7 mL/mL
- Dosage form
- Gel
- Route
- Topical
- Labeler
- GOJO Industries, LLCNDC labeler code 21749
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 21749-713_5643056c-a2b5-b48a-e063-6394a90a6a5dSPL ID 5643056c-a2b5-b48a-e063-6394a90a6a5dSPL set ID 59b47629-8b4e-4084-8bc8-66c7e5599e9cRxCUI 581662UNII 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
N421749071302followed by a unit qualifier and the quantityPackage 21749-0713-02. 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 Hand sanitizer to help reduce bacteria on the skin
Excerpt only. Read the full label for complete information.
About NDC 21749-713
- What is NDC 21749-713?
- 21749-713 is the product NDC for Purell Advanced Soothing (alcohol), Alcohol .7 mL/mL gel, listed with the FDA by GOJO Industries, LLC. It has 8 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Purell Advanced Soothing (Alcohol).
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- GOJO Industries, LLC, NDC labeler code 21749. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Purell Advanced Soothing?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
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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