ULTRA PRO - 55924-2001-1 - (artemisia abrotanum flowering top, semecarpus anacardium juice, barium chloride dihydrate, oyster shell calcium carbonate, crude, tribasic calcium phosphate, fucus vesiculosus, graphite, helleborus niger root, bos taurus hypothalamus, strychnos ignatii seed, lycopodium clavatum spore, magnesium phosphate, dibasic trihydrate, claviceps purpurea sclerotium, silicon dioxide, solidago virgaurea flowering top, thymus serpyllum and thyroid, unspecified)

Alphabetical Index


Drug Information of ULTRA PRO

Product NDC: 55924-2001
Proprietary Name: ULTRA PRO
Non Proprietary Name: artemisia abrotanum flowering top, semecarpus anacardium juice, barium chloride dihydrate, oyster shell calcium carbonate, crude, tribasic calcium phosphate, fucus vesiculosus, graphite, helleborus niger root, bos taurus hypothalamus, strychnos ignatii seed, lycopodium clavatum spore, magnesium phosphate, dibasic trihydrate, claviceps purpurea sclerotium, silicon dioxide, solidago virgaurea flowering top, thymus serpyllum and thyroid, unspecified
Active Ingredient(s): 10; 10; 15; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 15; 10    [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   artemisia abrotanum flowering top, semecarpus anacardium juice, barium chloride dihydrate, oyster shell calcium carbonate, crude, tribasic calcium phosphate, fucus vesiculosus, graphite, helleborus niger root, bos taurus hypothalamus, strychnos ignatii seed, lycopodium clavatum spore, magnesium phosphate, dibasic trihydrate, claviceps purpurea sclerotium, silicon dioxide, solidago virgaurea flowering top, thymus serpyllum and thyroid, unspecified
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ULTRA PRO

Product NDC: 55924-2001
Labeler Name: SENA LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130301

Package Information of ULTRA PRO

Package NDC: 55924-2001-1
Package Description: 1 mL in 1 BOTTLE (55924-2001-1)

NDC Information of ULTRA PRO

NDC Code 55924-2001-1
Proprietary Name ULTRA PRO
Package Description 1 mL in 1 BOTTLE (55924-2001-1)
Product NDC 55924-2001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name artemisia abrotanum flowering top, semecarpus anacardium juice, barium chloride dihydrate, oyster shell calcium carbonate, crude, tribasic calcium phosphate, fucus vesiculosus, graphite, helleborus niger root, bos taurus hypothalamus, strychnos ignatii seed, lycopodium clavatum spore, magnesium phosphate, dibasic trihydrate, claviceps purpurea sclerotium, silicon dioxide, solidago virgaurea flowering top, thymus serpyllum and thyroid, unspecified
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20130301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name SENA LLC
Substance Name ARTEMISIA ABROTANUM FLOWERING TOP; BARIUM CHLORIDE DIHYDRATE; BOS TAURUS HYPOTHALAMUS; CLAVICEPS PURPUREA SCLEROTIUM; FUCUS VESICULOSUS; GRAPHITE; HELLEBORUS NIGER ROOT; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEMECARPUS ANACARDIUM JUICE; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS IGNATII SEED; THYMUS SERPYLLUM; THYROID, UNSPECIFIED; TRIBASIC CALCIUM PHOSPHATE
Strength Number 10; 10; 15; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 15; 10
Strength Unit [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of ULTRA PRO


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