HaliTonic - 68703-006-80 - (Carduus mar, Kali phos, Nat sulphuricum, Nux vom, Silicea, Acacia gum, Lactose, Magnesium stearate, Corn starch, Sucrose.)

Alphabetical Index


Drug Information of HaliTonic

Product NDC: 68703-006
Proprietary Name: HaliTonic
Non Proprietary Name: Carduus mar, Kali phos, Nat sulphuricum, Nux vom, Silicea, Acacia gum, Lactose, Magnesium stearate, Corn starch, Sucrose.
Active Ingredient(s): 6; 6; 3; 6; 3    [hp_C]/1; [hp_C]/1; [hp_X]/1; [hp_C]/1; [hp_X]/1 & nbsp;   Carduus mar, Kali phos, Nat sulphuricum, Nux vom, Silicea, Acacia gum, Lactose, Magnesium stearate, Corn starch, Sucrose.
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of HaliTonic

Product NDC: 68703-006
Labeler Name: Native Remedies LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121228

Package Information of HaliTonic

Package NDC: 68703-006-80
Package Description: 180 TABLET in 1 BOTTLE, GLASS (68703-006-80)

NDC Information of HaliTonic

NDC Code 68703-006-80
Proprietary Name HaliTonic
Package Description 180 TABLET in 1 BOTTLE, GLASS (68703-006-80)
Product NDC 68703-006
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Carduus mar, Kali phos, Nat sulphuricum, Nux vom, Silicea, Acacia gum, Lactose, Magnesium stearate, Corn starch, Sucrose.
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121228
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Native Remedies LLC
Substance Name POTASSIUM PHOSPHATE, DIBASIC; SILICON DIOXIDE; SILYBUM MARIANUM SEED; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED
Strength Number 6; 6; 3; 6; 3
Strength Unit [hp_C]/1; [hp_C]/1; [hp_X]/1; [hp_C]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of HaliTonic


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