Cal-5-revive Liquid
NDC Package 64616-109-02
Package Information
Cal-5-revive (calcium balance) liquids is classified as a
- allergens - [cs]
- bismuth - [cs]
- bismuth - [epc] (established pharmacologic class)
- blood coagulation factor - [epc] (established pharmacologic class)
- calcium - [cs]
- calculi dissolution agent - [epc] (established pharmacologic class)
- cations administered via oral route. This formulation utilizes a liquid delivery system. Marketed by Vitality Works, Inc., this product is identified by NDC 64616-109.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS 20 [hp_X]/mL
- BISMUTH SUBNITRATE 15 [hp_X]/mL
- CALCIUM ARSENATE 12 [hp_X]/mL
- CALCIUM FLUORIDE 25 [hp_X]/mL
- CALCIUM HYDROXIDE 27 [hp_X]/mL
- CALCIUM IODIDE 10 [hp_X]/mL
- CALCIUM OXALATE MONOHYDRATE 30 [hp_X]/mL
- ELAEIS GUINEENSIS FRUIT 20 [hp_X]/mL
- HELIANTHUS ANNUUS FLOWERING TOP 22 [hp_X]/mL
- HYDRANGEA ARBORESCENS ROOT 14 [hp_X]/mL
- IPECAC 24 [hp_X]/mL
- IRIS GERMANICA VAR. FLORENTINA ROOT 23 [hp_X]/mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 22 [hp_X]/mL
- MANGANESE ACETATE TETRAHYDRATE 22 [hp_X]/mL
- MERCURIUS SOLUBILIS 30 [hp_X]/mL
- OSMIUM 22 [hp_X]/mL
- PHOSPHORIC ACID 36 [hp_X]/mL
- POTASSIUM ARSENITE ANHYDROUS 20 [hp_X]/mL
- POTASSIUM CHLORATE 30 [hp_X]/mL
- SANGUINARINE NITRATE 17 [hp_X]/mL
- TELLURIUM 27 [hp_X]/mL
- ZINC GLUCONATE 30 [hp_X]/mL
- Allergens - [CS]
- Bismuth - [CS]
- Bismuth - [EPC] (Established Pharmacologic Class)
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cations, Divalent - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Plant Proteins - [CS]
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
Regulatory & Marketing
Hierarchy Structure
- 64616 - Vitality Works, Inc.
- 64616-109 - Cal-5-revive
- 64616-109-02 - 59 mL in 1 BOTTLE, DROPPER
- 64616-109 - Cal-5-revive
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 64616-109-02 identifies a specific commercial package of 59 ml in 1 bottle, dropper of Cal-5-revive, a human over the counter drug labeled by Vitality Works, Inc.. This liquid is formulated for oral use and contains aconitum napellus; bismuth subnitrate; calcium arsenate; calcium fluoride; calcium hydroxide; calcium iodide; calcium oxalate monohydrate; elaeis guineensis fruit; helianthus annuus flowering top; hydrangea arborescens root; ipecac; iris germanica var. florentina root; magnesium phosphate, dibasic trihydrate; manganese acetate tetrahydrate; mercurius solubilis; osmium; phosphoric acid; potassium arsenite anhydrous; potassium chlorate; sanguinarine nitrate; tellurium; zinc gluconate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Vitality Works, Inc. on March 20, 2013. The current certification is valid through December 31, 2026.
How is this Vitality Works, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 64616010902. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.