CardCare NDC 55714-4853

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-4853Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-4853Add 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
55714-4853-1	55714485301	30 mL in 1 BOTTLE, GLASS (55714-4853-1)Marketed from Sep 25, 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): CardCare
Generic name (nonproprietary): echinacea, hypericum, valeriana, aconitum nap., arsenicum alb., aur. met., baryta carb., benzoicum ac., berber. vulg., bryonia, calc. fluor., cantharis, ceanothus, chelidonium maj., chionanthus, cinchona, convallaria, crotalus hor., digitalis, gelsemium, glonoinum, hydrofluoricum ac. kali iod., lachesis, lycopus, naja, nux vom., phos., pulsatilla, rhus tox., vipera, elaps.
Active ingredients: Lycopus virginicus — 15 [hp_X]/mLAnemone pulsatilla — 15 [hp_X]/mLVipera berus venom — 16 [hp_X]/mLEchinacea, Unspecified — 6 [hp_X]/mLHypericum perforatum — 6 [hp_X]/mLAconitum napellus — 15 [hp_X]/mLBarium carbonate — 15 [hp_X]/mLValerian — 6 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLArsenic trioxide — 15 [hp_X]/mLBenzoic acid — 15 [hp_X]/mLChelidonium majus — 15 [hp_X]/mLHydrofluoric acid — 15 [hp_X]/mLPotassium iodide — 15 [hp_X]/mLLachesis muta venom — 15 [hp_X]/mLStrychnos nux-vomica seed — 15 [hp_X]/mLMicrurus corallinus venom — 30 [hp_X]/mLLytta vesicatoria — 15 [hp_X]/mLCeanothus americanus leaf — 15 [hp_X]/mLChionanthus virginicus bark — 15 [hp_X]/mLConvallaria majalis — 15 [hp_X]/mLDigitalis — 15 [hp_X]/mLNitroglycerin — 15 [hp_X]/mLNaja naja venom — 15 [hp_X]/mLCalcium fluoride — 15 [hp_X]/mLGold — 15 [hp_X]/mLBerberis vulgaris root bark — 15 [hp_X]/mLCinchona officinalis bark — 15 [hp_X]/mLCrotalus horridus horridus venom — 15 [hp_X]/mLGelsemium sempervirens root — 15 [hp_X]/mLPhosphorus — 15 [hp_X]/mLToxicodendron pubescens leaf — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 25, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 55714-4853_0634351f-fae4-a8e3-e063-6294a90a3b60SPL ID 0634351f-fae4-a8e3-e063-6294a90a3b60SPL set ID 06342201-f0b4-de0d-e063-6294a90a5621UNII TWH5125Q6F, I76KB35JEV, 0ORO6NCA4M, 4N9P6CC1DX, XK4IUX8MNB, U0NQ8555JD, 6P669D8HQ8, JWF5YAW3QW, T7J046YI2B, S7V92P67HO, 8SKN0B0MIM, 7E889U5RNN, RGL5YE86CZ, 1C4QK22F9J, VSW71SS07I, 269XH13919, V0S6H36980, 3Q034RO3BT, 25B1Y14T8N, QHH4HVF5QE, F1T8QT9U8B, G59M7S0WS3, ZZ4AG7L7VM, O3B55K4YKI, 79Y1949PYO, 1TH8Q20J0U, S003A158SB, YHA2XLJ956, 639KR60Q1Q, 27YLU75U4W, 6IO182RP7A
Pharmacologic class: Nitrate Vasodilator; Nitrogen Binding Agent; Non-Standardized Plant Allergenic Extract; Standardized Chemical Allergen

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

N455714485301 followed by a unit qualifier and the quantity

Package 55714-4853-01. 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 Sep 25, 2023.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms such as fear, cold hands & feet, headache, weakness, sallow skin and palpitations.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)