Peacefuli NDC 71753-4001

NDC codes

FDA NDC Directory

Product NDC (as listed)71753-4001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71753-4001Add 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
71753-4001-1	71753400101	30 mL in 1 BOTTLE, SPRAY (71753-4001-1)Marketed from Mar 23, 2020

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): Peacefuli
Generic name (nonproprietary): avena sativa, humulus lupulus, passiflora incarnata, kali phosphoricum, anacardium orientale, argentum nitricum, ignatia amara
Active ingredients: Avena sativa flowering top — 3 [hp_X]/mLHops — 3 [hp_X]/mLPassiflora incarnata flowering top — 3 [hp_X]/mLDibasic potassium phosphate — 6 [hp_X]/mLPhosphoric acid — 6 [hp_X]/mLSemecarpus anacardium juice — 6 [hp_C]/mLSilver nitrate — 6 [hp_C]/mLStrychnos ignatii seed — 6 [hp_C]/mL
Dosage form: Spray
Route: Oral
Labeler: Ratis, LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 23, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 71753-4001_a8612e96-b081-4670-9de0-810bceee06bbSPL ID a8612e96-b081-4670-9de0-810bceee06bbSPL set ID eb3bc662-3d3d-4e4d-8561-330ad0eb08f2UNII MA9CQJ3F7F, 01G73H6H83, CLF5YFS11O, CI71S98N1Z, E4GA8884NN, Y0F0BU8RDU, 95IT3W8JZE, 1NM3M2487KUPC 0371753400110
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471753400101 followed by a unit qualifier and the quantity

Package 71753-4001-01. 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 May 25, 2023.

Indications (excerpt from the label)

USES: May temporarily relieve anxiousness, stress, and physical exhaustion and help you sleep.* *Claims based on traditional homeopathic practice, not accepted medial evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)