Bruise RX NDC 82734-0001

NDC codes

FDA NDC Directory

Product NDC (as listed)82734-0001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82734-0001Add 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
82734-0001-1	82734000101	30 mL in 1 BOTTLE, DROPPER (82734-0001-1)Marketed from Aug 10, 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): Bruise RXSuffix: RX
Generic name (nonproprietary): erigeron canadensis, hamamelis virginiana, phosphorus, sulphuricum acidum, arnica montana, ledum palustre, bellis perennis
Active ingredients: Erigeron canadensis whole — 30 [hp_X]/mLHamamelis virginiana root bark/stem bark — 6 [hp_C]/mLPhosphorus — 6 [hp_C]/mLSulfuric acid — 9 [hp_C]/mLArnica montana whole — 12 [hp_C]/mLRhododendron tomentosum leafy twig — 12 [hp_C]/mLBellis perennis whole — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Remedies Cure, LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 10, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 82734-0001_f7b9f15a-d9a4-4ab8-a993-41c7565344cfSPL ID f7b9f15a-d9a4-4ab8-a993-41c7565344cfSPL set ID 8fbac9c7-45ac-4a9b-bdff-6f19d238a601UNII 16D08B0B9N, T7S323PKJS, 27YLU75U4W, O40UQP6WCF, O80TY208ZW, 877L01IZ0P, 2HU33I03UY

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

N482734000101 followed by a unit qualifier and the quantity

Package 82734-0001-01. 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 Aug 10, 2022.

Indications (excerpt from the label)

INDICATIONS: May aid in the resolution of bruising caused by cosmetic injections, minor surgery and minor trauma.** **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)