Total Pro-Jes NDC 61657-0974

NDC codes

FDA NDC Directory

Product NDC (as listed)61657-0974Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61657-0974Add 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
61657-0974-1	61657097401	30 mL in 1 BOTTLE, DROPPER (61657-0974-1)Marketed from Sep 15, 2011

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): Total Pro-Jes
Generic name (nonproprietary): adrenal,belladonna,chelidonium,dioscoreavillosa,folliculinum,hypothalamus,arginine,liliumtigrinium,liver,oophorinum,pineal,pituitarinum,placentanium,progesterone
Active ingredients: Progesterone — 6 [hp_C]/30mLEpinephrine — 6 [hp_C]/30mLAtropa belladonna — 6 [hp_C]/30mLChelidonium majus — 6 [hp_C]/30mLDioscorea villosa root — 6 [hp_C]/30mLEstrone — 6 [hp_C]/30mLBos taurus hypothalamus — 6 [hp_C]/30mLArginine — 6 [hp_X]/30mLLilium lancifolium flowering top — 12 [hp_C]/30mLMammal liver — 6 [hp_C]/30mLSus scrofa ovary — 6 [hp_C]/30mLBos taurus pineal gland — 6 [hp_X]/30mLBos taurus pituitary gland — 6 [hp_X]/30mLSus scrofa placenta — 6 [hp_X]/30mLPulsatilla vulgaris — 12 [hp_C]/30mLSepia officinalis juice — 12 [hp_C]/30mLSulfur — 12 [hp_C]/30mL
Dosage form: Liquid
Route: Oral
Labeler: White Manufacturing Inc. BDA Micro-West
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 15, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Catecholamines (Chemical structure)Progesterone (Chemical structure)
Identifiers: Product ID 61657-0974_b9702889-9e53-da42-e053-2995a90a45deSPL ID b9702889-9e53-da42-e053-2995a90a45deSPL set ID b26953f8-7b56-432c-958c-d80c528fbb6aUNII 4G7DS2Q64Y, YKH834O4BH, WQZ3G9PF0H, 7E889U5RNN, IWY3IWX2G8, 2DI9HA706A, S6G2NLH4Y7, 94ZLA3W45F, 6268MFA917, S7YTV04R8O, Z7RM5NBH36, 7JM57I419K, C8CV8867O8, I76KB35JEV, QDL83WN8C2, 70FD1KFU70
Pharmacologic class: Catecholamine; Progesterone; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N461657097401 followed by a unit qualifier and the quantity

Package 61657-0974-01. 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 Jan 21, 2021.

Indications (excerpt from the label)

INDICATIONS INDICATIONS: For the temporary relief of hot flashes, irritable disposition, liver, uterine, vaginal and sleep complaints.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)