NDC 63479-0101 A01 Cellular Recharge
Aceticum Acidum,Arnica Montana,Avena Sativa,Calcarea Carbonica,Calcarea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63479 - Apex Energetics Inc.
- 63479-0101 - A01
Product Packages
NDC Code 63479-0101-1
Package Description: 30 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 63479-0101?
What are the uses for A01 Cellular Recharge?
What are A01 Cellular Recharge Active Ingredients?
- ACETIC ACID 30 [hp_X]/mL - Product of the oxidation of ethanol and of the destructive distillation of wood. It is used locally, occasionally internally, as a counterirritant and also as a reagent. (Stedman, 26th ed)
- ANHYDROUS CITRIC ACID 30 [hp_X]/mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
- ARNICA MONTANA 12 [hp_C]/mL
- AVENA SATIVA FLOWERING TOP 1 [hp_X]/mL
- CALCIUM SULFATE ANHYDROUS 12 [hp_X]/mL
- CARPINUS BETULUS FLOWER 9 [hp_X]/mL
- CEANOTHUS AMERICANUS LEAF 4 [hp_X]/mL
- CERATOSTIGMA WILLMOTTIANUM FLOWER 12 [hp_X]/mL
- GENTIANELLA AMARELLA FLOWER 12 [hp_X]/mL
- HYDROFLUORIC ACID 30 [hp_X]/mL - Hydrofluoric acid. A solution of hydrogen fluoride in water. It is a colorless fuming liquid which can cause painful burns.
- JUGLANS REGIA FLOWERING TOP 9 [hp_X]/mL
- LACTIC ACID, DL- 15 [hp_X]/mL
- LACTIC ACID, L- 15 [hp_X]/mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 15 [hp_X]/mL
- OLEA EUROPAEA FLOWER 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 15 [hp_X]/mL
- PASSIFLORA INCARNATA FLOWERING TOP 1 [hp_X]/mL
- PHOSPHORIC ACID 30 [hp_X]/mL
- QUININE ARSENITE 15 [hp_X]/mL
- SODIUM CHLORIDE 30 [hp_X]/mL - A ubiquitous sodium salt that is commonly used to season food.
- SODIUM HEXAFLUOROSILICATE 8 [hp_X]/mL
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/mL
- SODIUM SULFATE 10 [hp_X]/mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 1 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 15 [hp_X]/mL
- ULMUS PROCERA FLOWERING TWIG 12 [hp_X]/mL
Which are A01 Cellular Recharge UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CERATOSTIGMA WILLMOTTIANUM FLOWER (UNII: TP69J995TW)
- CERATOSTIGMA WILLMOTTIANUM FLOWER (UNII: TP69J995TW) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
- GENTIANELLA AMARELLA FLOWER (UNII: ZKH2SOY1AR)
- GENTIANELLA AMARELLA FLOWER (UNII: ZKH2SOY1AR) (Active Moiety)
- ULMUS PROCERA FLOWERING TWIG (UNII: J3O020I532)
- ULMUS PROCERA FLOWERING TWIG (UNII: J3O020I532) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- CARPINUS BETULUS FLOWER (UNII: 07YL55QKZ9)
- CARPINUS BETULUS FLOWER (UNII: 07YL55QKZ9) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- ACETIC ACID (UNII: Q40Q9N063P)
- ACETIC ACID (UNII: Q40Q9N063P) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N)
- CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N) (Active Moiety)
- SODIUM HEXAFLUOROSILICATE (UNII: 806AV2E065)
- QUININE ARSENITE (UNII: 42QO5P0NLM)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (Active Moiety)
Which are A01 Cellular Recharge Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for A01 Cellular Recharge?
- Acidifying Activity - [MoA] (Mechanism of Action)
- Anti-coagulant - [EPC] (Established Pharmacologic Class)
- Antimalarial - [EPC] (Established Pharmacologic Class)
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium Chelating Activity - [MoA] (Mechanism of Action)
- Calcium - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cations, Divalent - [CS]
- Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Coagulation Factor Activity - [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)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".