NDC codes

FDA NDC Directory
Product NDC (as listed)87710-002Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87710-0002Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
87710-002-01877100002011 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

Generic name (nonproprietary)
0.9% benzyl alcohol solution (laboratory use only)
Active ingredients
Benzyl alcohol — .9 mg/100mg
Dosage form
Liquid
Route
Cutaneous
Labeler
Guangzhou Huanmei Cosmetics Co., LtdNDC labeler code 87710
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

N487710000201 followed by a unit qualifier and the quantity

Package 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Bacteriostatic Water with 0.9% Benzyl Alcohol is intended for research use only. It may be used in research applications as a bacteriostatic solution to inhibit bacterial and mould growth, as a solubilizer to dissolve peptides and lipophilic active ingredients and help prevent stratification, as a penetration aid for in vitro penetration testing, and as an irritation buffer to reduce irritation associated with high-concentration raw materials. This product is not intended for injection, skin application, or oral intake.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87710-002

What is NDC 87710-002?
87710-002 is the product NDC for 0.9% Benzyl Alcohol Solution (Laboratory Use Only), Benzyl alcohol .9 mg/100mg liquid, listed with the FDA by Guangzhou Huanmei Cosmetics Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
0.9% Benzyl Alcohol Solution (Laboratory Use Only).
What is the active ingredient?
Benzyl alcohol.
Who is the labeler?
Guangzhou Huanmei Cosmetics Co., Ltd, NDC labeler code 87710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for 0.9% Benzyl Alcohol Solution (Laboratory Use Only)?
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.

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