Psora Miasm NDC 44911-0668

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0668Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0668Add 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
44911-0668-1	44911066801	30 mL in 1 BOTTLE, DROPPER (44911-0668-1)Marketed from Mar 15, 2023

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): Psora Miasm
Generic name (nonproprietary): eggshell membrane, whey protein, calcarea carbonica, lycopodium clavatum, sulphur, arsenicum album, fagopyrum esculentum, graphites, hydrocotyle asiatica, natrum muriaticum
Active ingredients: Egg shell membrane — 6 [hp_X]/mLWhey — 6 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLSulfur — 30 [hp_X]/mLArsenic trioxide — 12 [hp_C]/mLFagopyrum esculentum whole — 12 [hp_C]/mLGraphite — 12 [hp_C]/mLCentella asiatica whole — 12 [hp_C]/mLSodium chloride — 12 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 15, 2023
Marketing end: Apr 18, 2028
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Milk Proteins (Chemical structure)
Identifiers: Product ID 44911-0668_4e0d573c-9b1c-4cf5-ba91-2ee03b781f6aSPL ID 4e0d573c-9b1c-4cf5-ba91-2ee03b781f6aSPL set ID d008a091-b7c6-41f1-a1cf-f8224ebe55e5UNII N7QBR4212V, 8617Z5FMF6, 2E32821G6I, C88X29Y479, 70FD1KFU70, S7V92P67HO, B10M69172N, 4QQN74LH4O, 7M867G6T1U, 451W47IQ8XUPC 0363113701036
Pharmacologic class: Non-Standardized Food 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911066801 followed by a unit qualifier and the quantity

Package 44911-0668-01. 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 Oct 29, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve: • itching of the skin • eruption on the scalp and bends of joints with itching • skin that is dry, scaly • general exhaustion.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)