A01 Cellular Recharge NDC 63479-0101

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0101Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0101Add 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
63479-0101-1	63479010101	30 mL in 1 BOTTLE, GLASS (63479-0101-1)Marketed from Dec 15, 1994

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): A01 Cellular RechargeSuffix: CELLULAR RECHARGE
Generic name (nonproprietary): aceticum acidum, arnica montana, avena sativa, calcarea carbonica, calcarea phosphorica, calcarea sulphurica, ceanothus americanus, ceratostigma illmottianum, chininum arsenicosum, citricum acidum, english elm, european hornbeam, european olive, gentianella amarella, hydrofluoricum acidum, juglans regia, lacticum acidum, magnesia phosphorica, natrum muriaticum, natrum phosphoricum, natrum silicofluoricum, natrum sulphuricum, passiflora incarnata, phosphoricum acidum, sarcolacticum acidum, solidago virgaurea
Active ingredients: Calcium sulfate anhydrous — 12 [hp_X]/mLCeratostigma willmottianum flower — 12 [hp_X]/mLLactic acid, L- — 15 [hp_X]/mLArnica montana — 12 [hp_C]/mLOyster shell calcium carbonate, Crude — 15 [hp_X]/mLAnhydrous citric acid — 30 [hp_X]/mLOlea europaea flower — 12 [hp_X]/mLGentianella amarella flower — 12 [hp_X]/mLUlmus procera flowering twig — 12 [hp_X]/mLSodium phosphate, Dibasic, Heptahydrate — 12 [hp_X]/mLPhosphoric acid — 30 [hp_X]/mLCarpinus betulus flower — 9 [hp_X]/mLSolidago virgaurea flowering top — 1 [hp_X]/mLAcetic acid — 30 [hp_X]/mLAvena sativa flowering top — 1 [hp_X]/mLSodium chloride — 30 [hp_X]/mLTribasic calcium phosphate — 15 [hp_X]/mLCeanothus americanus leaf — 4 [hp_X]/mLSodium hexafluorosilicate — 8 [hp_X]/mLQuinine arsenite — 15 [hp_X]/mLHydrofluoric acid — 30 [hp_X]/mLJuglans regia flowering top — 9 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 15 [hp_X]/mLSodium sulfate — 10 [hp_X]/mLPassiflora incarnata flowering top — 1 [hp_X]/mLLactic acid, Dl- — 15 [hp_X]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 15, 1994
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Calcium (Chemical structure)Divalent (Chemical structure)Decreased Coagulation Factor Activity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63479-0101_0e7630cb-8c84-6d0e-e063-6394a90ace15SPL ID 0e7630cb-8c84-6d0e-e063-6394a90ace15SPL set ID b932ebd3-afea-6a95-e053-2995a90a2735UNII E934B3V59H, TP69J995TW, F9S9FFU82N, O80TY208ZW, 2E32821G6I, XF417D3PSL, 498M34P1VZ, ZKH2SOY1AR, J3O020I532, 70WT22SF4B, E4GA8884NN, 07YL55QKZ9, 5405K23S50, Q40Q9N063P, MA9CQJ3F7F, 451W47IQ8X, 91D9GV0Z28, 25B1Y14T8N, 806AV2E065, 42QO5P0NLM, RGL5YE86CZ, 3BA2N709NG, HF539G9L3Q, 0YPR65R21J, CLF5YFS11O, 3B8D35Y7S4UPC 0818960011109
Pharmacologic class: Anti-coagulant; Antimalarial; Blood Coagulation Factor; Calculi Dissolution Agent; Osmotic Laxative; Phosphate Binder

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463479010101 followed by a unit qualifier and the quantity

Package 63479-0101-01. 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 Jan 8, 2024.

Indications (excerpt from the label)

Uses: For temporary relief of minor: fatigue* irritability* cramps* exhaustion* restlessness* *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)