NDC 68703-006

HaliTonic

Carduus Mar, Kali Phos, Nat Sulphuricum, Nux Vom, Silicea, Acacia Gum, Lactose, Magnesium Stearate, Corn Starch, Sucrose.

HaliTonic is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Native Remedies Llc. The primary component is Silybum Marianum Seed; Potassium Phosphate, Dibasic; Sodium Sulfate; Strychnos Nux-vomica Seed; Silicon Dioxide.

• Product ID: 68703-006_5481ad2f-e078-4036-8014-691daf4041c9
• NDC: 68703-006
• Product Type: Human Otc Drug
• Proprietary Name: HaliTonic
• Generic Name: Carduus Mar, Kali Phos, Nat Sulphuricum, Nux Vom, Silicea, Acacia Gum, Lactose, Magnesium Stearate, Corn Starch, Sucrose.
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2012-12-28
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Native Remedies LLC
• Substance Name: SILYBUM MARIANUM SEED; POTASSIUM PHOSPHATE, DIBASIC; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; SILICON DIOXIDE
• Active Ingredient Strength: 3 [hp_X]/1; [hp_C]/1; [hp_C]/1; [hp_X]/1; [hp_C]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 68703-006-80

180 TABLET in 1 BOTTLE, GLASS (68703-006-80)

• Marketing Start Date: 2012-12-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68703-006-80 [68703000680]

HaliTonic TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-12-28
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SILYBUM MARIANUM SEED	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: a92356e8-9112-4184-a3c8-403859633892
• Manufacturer:
  • Native Remedies LLC
• UNII:
  • ETJ7Z6XBU4
  • 269XH13919
  • 0YPR65R21J
  • CI71S98N1Z
  • U946SH95EE
• UPC Code:
  • 0810845011280