Over-the-counter drug · UNAPPROVED DRUG OTHER
0.9% Benzyl Alcohol Solution (Laboratory Use Only) NDC 87710-002
Benzyl alcohol .9 mg/100mg · Liquid · Cutaneous · Guangzhou Huanmei Cosmetics Co., Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87710-002-01 | 87710000201 | 1 BOTTLE in 1 BOX (87710-002-01) / 30 mg in 1 BOTTLEMarketed from Aug 20, 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)
- 0.9% Benzyl Alcohol Solution (Laboratory Use Only)
- Generic name (nonproprietary)
- 0.9% benzyl alcohol solution (laboratory use only)
- Active ingredients
- Benzyl alcohol — .9 mg/100mg
- Dosage form
- Liquid
- Route
- Cutaneous
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 87710-002_5976bde6-099a-ffc4-e063-6394a90aadcfSPL ID 5976bde6-099a-ffc4-e063-6394a90aadcfSPL set ID 5976bde6-0999-ffc4-e063-6394a90aadcfUNII LKG8494WBH
- Pharmacologic class
- Pediculicide
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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N487710000201followed by a unit qualifier and the quantityPackage 87710-0002-01. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.