Over-the-counter drug · OTC MONOGRAPH DRUG
Youmi Alcohol Prep Pad 70 Isopropyl Alcohol (Isopropyl alcohol) NDC 87401-000
Isopropyl alcohol 70 mL/100mL · Liquid · Topical · PT YOUMI MEDIKA INDUSTRI
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87401-000-00 | 8740100000087401000000 | .34 mL in 1 POUCH (87401-000-00)Marketed from Feb 5, 2026 |
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)
- Youmi Alcohol Prep Pad 70 Isopropyl Alcohol
- Generic name (nonproprietary)
- isopropyl alcohol
- Active ingredients
- Isopropyl alcohol — 70 mL/100mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- PT YOUMI MEDIKA INDUSTRINDC labeler code 87401
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 87401-000_4a6ad128-ef29-63c0-e063-6394a90ab3e3SPL ID 4a6ad128-ef29-63c0-e063-6394a90ab3e3SPL set ID e3b1a576-a8eb-44bf-8f9c-a49a44a894e8RxCUI 797544UNII ND2M416302
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
N487401000000followed by a unit qualifier and the quantityPackage 87401-0000-00. 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 preparation of the skin prior to an injection.
Excerpt only. Read the full label for complete information.
About NDC 87401-000
- What is NDC 87401-000?
- 87401-000 is the product NDC for Youmi Alcohol Prep Pad 70 Isopropyl Alcohol, Isopropyl alcohol 70 mL/100mL liquid, listed with the FDA by PT YOUMI MEDIKA INDUSTRI. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Youmi Alcohol Prep Pad 70 Isopropyl Alcohol (Isopropyl alcohol).
- What is the active ingredient?
- Isopropyl alcohol.
- Who is the labeler?
- PT YOUMI MEDIKA INDUSTRI, NDC labeler code 87401. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Youmi Alcohol Prep Pad 70 Isopropyl Alcohol?
- 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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