Over-the-counter drug · OTC MONOGRAPH DRUG
PURELL Advanced E3 Rated Instant Hand Sanitizer Foam (Alcohol) NDC 21749-802
Alcohol .7 mL/mL · Liquid · Topical · GOJO Industries, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 21749-802-89 | 2174908028921749080289 | 1200 mL in 1 BOTTLE (21749-802-89)Marketed from Jun 1, 2012 |
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 E3 Rated Instant Hand Sanitizer Foam
- Generic name (nonproprietary)
- alcohol
- Active ingredients
- Alcohol — .7 mL/mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- GOJO Industries, Inc.NDC labeler code 21749
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 21749-802_2916dce7-fee4-552c-e063-6294a90a5cb5SPL ID 2916dce7-fee4-552c-e063-6294a90a5cb5SPL set ID 1f78370b-132a-4759-8cbc-b5e093f90f8dRxCUI 616805UNII 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
N421749080289followed by a unit qualifier and the quantityPackage 21749-0802-89. 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 that cause disease Recommended for repeated use
Excerpt only. Read the full label for complete information.
About NDC 21749-802
- What is NDC 21749-802?
- 21749-802 is the product NDC for PURELL Advanced E3 Rated Instant Hand Sanitizer Foam, Alcohol .7 mL/mL liquid, listed with the FDA by GOJO Industries, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- PURELL Advanced E3 Rated Instant Hand Sanitizer Foam (Alcohol).
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- GOJO Industries, Inc., 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 E3 Rated Instant Hand Sanitizer Foam?
- 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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