HOMWIS Anti-itch Cream NDC 73076-507

NDC codes

FDA NDC Directory

Product NDC (as listed)73076-507Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73076-0507Add 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
73076-507-02	73076050702	50 g in 1 JAR (73076-507-02)Marketed from Dec 1, 2022
73076-507-03	73076050703	100 g in 1 JAR (73076-507-03)Marketed from Dec 1, 2022

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): HOMWIS Anti-itch Cream
Generic name (nonproprietary): homwis anti-itch cream
Active ingredients: Oatmeal — 1 g/100g
Dosage form: Cream
Route: Topical
Labeler: Shenzhen Ishan Technology Co., Ltd
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Dec 1, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Grain Proteins (EXT)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 73076-507_5b1a689f-c608-2fed-e063-6394a90ae629SPL ID 5b1a689f-c608-2fed-e063-6394a90ae629SPL set ID 5b1a68f5-5f5d-7e1a-e063-6294a90a8a92RxCUI 240651UNII 8PI54V663Y
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N473076050702 followed by a unit qualifier and the quantity

Package 73076-0507-02. 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 Sep 10, 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)