Relaxoforce NDC 43857-0545

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0545Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0545Add 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
43857-0545-1	43857054501	30 mL in 1 BOTTLE, DROPPER (43857-0545-1)Marketed from Feb 19, 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): Relaxoforce
Generic name (nonproprietary): humulus lupulus, passiflora incarnata, valeriana officinalis, calcarea carbonica, coffea tosta, ignatia amara, kali phosphoricum, moschus, nux vomica, phosphorus, pulsatilla (pratensis)
Active ingredients: Hops — 3 [hp_X]/mLPassiflora incarnata flowering top — 3 [hp_X]/mLValerian — 3 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLCoffea arabica seed, Roasted — 12 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLDibasic potassium phosphate — 12 [hp_X]/mLMoschus moschiferus musk sac resin — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 19, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43857-0545_a57d489a-e899-49a0-a47a-c8a134322b2aSPL ID a57d489a-e899-49a0-a47a-c8a134322b2aSPL set ID 141fb6b7-08d9-4b57-bafd-ba5c8f98914eUNII 01G73H6H83, CLF5YFS11O, JWF5YAW3QW, 2E32821G6I, 9H58JRT35E, 1NM3M2487K, CI71S98N1Z, 8KFK4W7KP7, 269XH13919, 27YLU75U4W, 8E272251DIUPC 0810184340027
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

N443857054501 followed by a unit qualifier and the quantity

Package 43857-0545-01. 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 Mar 11, 2026.

Indications (excerpt from the label)

USES: For temporary relief of anxiety and stress.** **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)