iShanCare Vaginal Antibacterial Gel NDC 73076-158

NDC codes

FDA NDC Directory

Product NDC (as listed)73076-158Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73076-0158Add 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 NDC	11-digit (billing)	Package	Copy
73076-158-01	73076015801	21 g in 1 TUBE (73076-158-01)Marketed from Oct 25, 2024

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): iShanCare Vaginal Antibacterial Gel
Generic name (nonproprietary): ishancare vaginal antibacterial gel
Active ingredients: Lactic acid — .02 g/100g
Dosage form: Cream
Route: Topical
Labeler: Shenzhen Ishan Technology Co., Ltd
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 25, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Acidifying Activity (Mechanism)
Identifiers: Product ID 73076-158_4aae6cc9-5e66-a716-e063-6294a90aaec1SPL ID 4aae6cc9-5e66-a716-e063-6294a90aaec1SPL set ID 254a6624-80b6-b089-e063-6294a90a887eUNII 33X04XA5ATUPC 6973496921538

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

N473076015801 followed by a unit qualifier and the quantity

Package 73076-0158-01. 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 Feb 12, 2026.

Indications (excerpt from the label)

Directions Wash and dry affected area, apply a thin layer of LMNOOP over affected area, gently massage until fully absorbed, repeat 2-3 times daily.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)