Over-the-counter drug · OTC MONOGRAPH DRUG
gumdrop glitz hand sanitizer (Alcohol) NDC 11673-868
Alcohol 620 mg/g · Gel · Topical · Target Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 11673-868-30 | 11673086830 | 30 g in 1 BOTTLE, PLASTIC (11673-868-30)Marketed from Aug 15, 2019 |
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)
- gumdrop glitz hand sanitizer
- Generic name (nonproprietary)
- alcohol
- Active ingredients
- Alcohol — 620 mg/g
- Dosage form
- Gel
- Route
- Topical
- Labeler
- Target CorporationNDC labeler code 11673
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 11673-868_089971c6-98d8-a75b-e063-6394a90a6a84SPL ID 089971c6-98d8-a75b-e063-6394a90a6a84SPL set ID c1731db5-34ac-4773-a99b-ac4eae7ab433RxCUI 581660UNII 3K9958V90MUPC 0829576060894
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
N411673086830followed by a unit qualifier and the quantityPackage 11673-0868-30. 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 for hand-washing to decrease bacteria on the skin, only when water is not available
Excerpt only. Read the full label for complete information.
About NDC 11673-868
- What is NDC 11673-868?
- 11673-868 is the product NDC for gumdrop glitz hand sanitizer (alcohol), Alcohol 620 mg/g gel, listed with the FDA by Target Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- gumdrop glitz hand sanitizer (Alcohol).
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- Target Corporation, NDC labeler code 11673. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for gumdrop glitz hand sanitizer?
- 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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