Vaxr Hc NDC 43742-2018

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2018Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2018Add 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
43742-2018-1	43742201801	30 mL in 1 BOTTLE, PLASTIC (43742-2018-1)Marketed from Dec 21, 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): Vaxr Hc
Generic name (nonproprietary): thuja occidentalis, mezereum, silicea, calcarea carbonica, morbillinum, parotidinum, pertussinum, rubella nosode, tetanus toxin, carcinosin, antimonium crudum, ledum palustre, thimerosal, poliomyelitis nosode
Active ingredients: Thuja occidentalis leafy twig — 6 [hp_X]/mLDaphne mezereum bark — 8 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLMeasles virus — 30 [hp_X]/mLMumps virus — 30 [hp_X]/mLBordetella pertussis — 30 [hp_X]/mLRubella virus — 30 [hp_X]/mLClostridium tetani — 30 [hp_X]/mLHuman breast tumor cell — 15 [hp_C]/mLAntimony trisulfide — 30 [hp_C]/mLLedum palustre twig — 30 [hp_C]/mLThimerosal — 30 [hp_C]/mLPoliovirus — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 21, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-2018_27e6d102-3362-4318-a704-3b497f7b001aSPL ID 27e6d102-3362-4318-a704-3b497f7b001aSPL set ID fdf8d21a-2ae1-4842-abf3-737841995939UNII 1NT28V9397, X2N6E405GV, ETJ7Z6XBU4, 2E32821G6I, HT3R7C012Q, YF0S03R447, 2QNL82089R, U751HEX436, 751E8J54VM, C62OO7VD9K, F79059A38U, 877L01IZ0P, 2225PI3MOV, FZJ641678TUPC 0810151881218

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

N443742201801 followed by a unit qualifier and the quantity

Package 43742-2018-01. 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 Apr 3, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • fever • headache • muscle pain • rash • cough • lethargy • aching back These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)