Over-the-counter drug · OTC MONOGRAPH DRUG
SunDrops 75 (Alcohol) NDC 63621-356
Alcohol .6 mL/mL · Gel · Topical · Sunburst Chemicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63621-356-14 | 6362103561463621035614 | 3785 mL in 1 BOTTLE, PLASTIC (63621-356-14)Marketed from May 7, 2020 | |
| 63621-356-20 | 6362103562063621035620 | 8 BAG in 1 BOX (63621-356-20) / 1000 mL in 1 BAGMarketed from Oct 14, 2009 | |
| 63621-356-25 | 6362103562563621035625 | 12 BOTTLE, PUMP in 1 BOX (63621-356-25) / 236.6 mL in 1 BOTTLE, PUMPMarketed from Oct 14, 2009 | |
| 63621-356-40 | 6362103564063621035640 | 4 BAG in 1 BOX (63621-356-40) / 1000 mL in 1 BAGMarketed from Oct 16, 2025 | |
| 63621-356-50 | 6362103565063621035650 | 473.2 mL in 1 BOTTLE, PUMP (63621-356-50)Marketed from Jun 29, 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)
- SunDrops 75
- Generic name (nonproprietary)
- alcohol
- Active ingredients
- Alcohol — .6 mL/mL
- Dosage form
- Gel
- Route
- Topical
- Labeler
- Sunburst Chemicals, Inc.NDC labeler code 63621
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 63621-356_435330fc-c021-151b-e063-6394a90a229bSPL ID 435330fc-c021-151b-e063-6394a90a229bSPL set ID b0623424-939e-4b49-aa99-c1ef22cf0f2dRxCUI 581658UNII 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
N463621035614followed by a unit qualifier and the quantityPackage 63621-0356-14. 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)
Use To help reduce amount of bacteria on the skin
Excerpt only. Read the full label for complete information.
About NDC 63621-356
- What is NDC 63621-356?
- 63621-356 is the product NDC for SunDrops 75 (alcohol), Alcohol .6 mL/mL gel, listed with the FDA by Sunburst Chemicals, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- SunDrops 75 (Alcohol).
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- Sunburst Chemicals, Inc., NDC labeler code 63621. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for SunDrops 75?
- 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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