Uterine Formula 2105 (uterine formula) NDC 63083-2105

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2105Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2105Add 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
63083-2105-2	63083210502	59 mL in 1 BOTTLE, DROPPER (63083-2105-2)Marketed from Aug 15, 1985

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Uterine Formula 2105Suffix: 2105
Generic name (nonproprietary): uterine formula
Active ingredients: Lindera aggregata root — 1 [hp_X]/59mLVitex negundo fruit — 1 [hp_X]/59mLAconitum carmichaeli lateral root — 3 [hp_X]/59mLCinnamomum cassia twig — 3 [hp_X]/59mLCrocus sativus flower — 3 [hp_X]/59mLPhellodendron chinensis bark — 3 [hp_X]/59mLCrassostrea gigas shell — 3 [hp_X]/59mLViscum album fruiting top — 3 [hp_X]/59mLAstragalus propinquus root — 6 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Identifiers: Product ID 63083-2105_b6ffdc9f-9570-4b8b-bb3d-a77236ac48d4SPL ID b6ffdc9f-9570-4b8b-bb3d-a77236ac48d4SPL set ID 0416d627-6ac8-4fcc-8f54-797ddfcaf3e7UNII 517Q7XRT2T, WR2NH7PU9S, 2A9PW94VJX, 4UD6VQR2UP, 00IF91KFKQ, 2866QMZ434, 5I0R0U8ZL0, BK9092J5MP, 922OP8YUPF

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083210502 followed by a unit qualifier and the quantity

Package 63083-2105-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of painful or heavy menses, abdominal cramping, or aches in back or legs.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)