NDC 66579-0075

Smoke Freee

Arsenicum Album, Caladium Seguinum, Carbolicum Acidum, Daphne Indica, Eugenia Jambosa, Kali Phosphoricum, Lobelia Inflata, Nicotinum, Nux Vomica, Plantago Major, Saccharum Officinale, Staphysagria, Tabacum, Thuja Occidentalis

Smoke Freee is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by New Sun Inc.. The primary component is Arsenic Trioxide; Dieffenbachia Seguine; Phenol; Daphne Odora Bark; Syzygium Jambos Seed; Potassium Phosphate, Dibasic; Lobelia Inflata; Nicotine; Strychnos Nux-vomica Seed; Plantago Major; Sucrose; Delphinium Staphisagria Seed; Tobacco Leaf; Thuja Occidentalis Leafy Twig.

• Product ID: 66579-0075_5d98074b-6d44-485a-816e-121b9043879c
• NDC: 66579-0075
• Product Type: Human Otc Drug
• Proprietary Name: Smoke Freee
• Generic Name: Arsenicum Album, Caladium Seguinum, Carbolicum Acidum, Daphne Indica, Eugenia Jambosa, Kali Phosphoricum, Lobelia Inflata, Nicotinum, Nux Vomica, Plantago Major, Saccharum Officinale, Staphysagria, Tabacum, Thuja Occidentalis
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-02-02
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: New Sun Inc.
• Substance Name: ARSENIC TRIOXIDE; DIEFFENBACHIA SEGUINE; PHENOL; DAPHNE ODORA BARK; SYZYGIUM JAMBOS SEED; POTASSIUM PHOSPHATE, DIBASIC; LOBELIA INFLATA; NICOTINE; STRYCHNOS NUX-VOMICA SEED; PLANTAGO MAJOR; SUCROSE; DELPHINIUM STAPHISAGRIA SEED; TOBACCO LEAF; THUJA OCCIDENTALIS LEAFY TWIG
• Active Ingredient Strength: 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 66579-0075-2

59 mL in 1 BOTTLE, SPRAY (66579-0075-2)

• Marketing Start Date: 2012-02-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 66579-0075-2 [66579007502]

Smoke Freee LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-02-02
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ARSENIC TRIOXIDE	10 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: e5e2f567-f6ca-43b0-98dd-4f164de8e1b8
• Manufacturer:
  • New Sun Inc.
• UNII:
  • 6M3C89ZY6R
  • 1NT28V9397
  • 9PP1T3TC5U
  • C151H8M554
  • S7V92P67HO
  • JSJ34YQJ5D
  • 6YR2608RSU
  • CI71S98N1Z
  • W2469WNO6U
  • 339NCG44TV
  • 97P0H45869
  • 01800C6E6B
  • 00543AP1JV
  • 269XH13919