MBM 13 Female NDC 50181-0084

NDC codes

FDA NDC Directory

Product NDC (as listed)50181-0084Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50181-0084Add 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
50181-0084-1	50181008401	30 mL in 1 BOTTLE, DROPPER (50181-0084-1)Marketed from May 3, 2022

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): MBM 13 Female
Generic name (nonproprietary): phytolacca decandra, hypophysis (suis), scrophularia nodosa, hypothalamus (suis), calcarea carbonica, cimicifuga racemosa, lilium tigrinum, sulphur, causticum, graphites, kali phosphoricum
Active ingredients: Phytolacca americana root — 3 [hp_C]/mLSus scrofa pituitary gland — 3 [hp_C]/mLScrophularia nodosa whole — 3 [hp_C]/mLBos taurus hypothalamus — 5 [hp_C]/mLOyster shell calcium carbonate, Crude — 89 [hp_C]/mLBlack cohosh — 89 [hp_C]/mLLilium lancifolium whole flowering — 89 [hp_C]/mLSulfur — 89 [hp_C]/mLCausticum — 144 [hp_C]/mLGraphite — 144 [hp_C]/mLDibasic potassium phosphate — 233 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: The Wellness Center for Research and Education, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 3, 2022
Marketing end: Jun 9, 2027
Identifiers: Product ID 50181-0084_35b365d2-28bc-4f96-93bc-6ea1fd171120SPL ID 35b365d2-28bc-4f96-93bc-6ea1fd171120SPL set ID 2ba45d16-58d8-4921-ae06-0cec43238dd3UNII 11E6VI8VEG, L0PFEMQ1DT, 7H443NUB2T, S6G2NLH4Y7, 2E32821G6I, K73E24S6X9, X67Z2963PI, 70FD1KFU70, DD5FO1WKFU, 4QQN74LH4O, CI71S98N1Z

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

N450181008401 followed by a unit qualifier and the quantity

Package 50181-0084-01. 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 Jun 6, 2025.

Indications (excerpt from the label)

INDICATIONS: For the temporary relief of emotionlessness, denial, numbness, and unresponsiveness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)