NDC 43742-0452

Breathe RxS

Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Natrum Muriaticum, Rhus Tox, Sulphur, Adenosinum Cyclophosphoricum, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Lung (suis), Mucosa Nasalis Suis, Sarcolacticum Acidum, Acetylcholine Chloride, Coumarinum, Malvin, Dysentery Bacillus, Morgan Bacillus (pure)

Breathe RxS is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Aconitum Napellus; Silver Nitrate; Arsenic Trioxide; Sodium Chloride; Toxicodendron Pubescens Leaf; Sulfur; Adenosine Cyclic Phosphate; Coenzyme A; Sus Scrofa Umbilical Cord; Sus Scrofa Adrenal Gland; Sus Scrofa Lung; Sus Scrofa Nasal Mucosa; Lactic Acid, L-; Acetylcholine Chloride; Coumarin; Malvin; Shigella Dysenteriae; Proteus Morganii.

• Product ID: 43742-0452_a3e8eefd-f532-49b5-9f47-74578e49ee1c
• NDC: 43742-0452
• Product Type: Human Otc Drug
• Proprietary Name: Breathe RxS
• Generic Name: Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Natrum Muriaticum, Rhus Tox, Sulphur, Adenosinum Cyclophosphoricum, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Lung (suis), Mucosa Nasalis Suis, Sarcolacticum Acidum, Acetylcholine Chloride, Coumarinum, Malvin, Dysentery Bacillus, Morgan Bacillus (pure)
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-03-11
• Marketing End Date: 2021-02-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: ACONITUM NAPELLUS; SILVER NITRATE; ARSENIC TRIOXIDE; SODIUM CHLORIDE; TOXICODENDRON PUBESCENS LEAF; SULFUR; ADENOSINE CYCLIC PHOSPHATE; COENZYME A; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; LACTIC ACID, L-; ACETYLCHOLINE CHLORIDE; COUMARIN; MALVIN; SHIGELLA DYSENTERIAE; PROTEUS MORGANII
• Active Ingredient Strength: 6 [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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0452-1

30 mL in 1 BOTTLE, DROPPER (43742-0452-1)

• Marketing Start Date: 2014-03-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0452-1 [43742045201]

Breathe RxS LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-03-11
• Marketing End Date: 2021-02-03

Drug Details

Active Ingredients

Ingredient	Strength
ACONITUM NAPELLUS	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 04f2642b-fd1c-4181-89c7-eace044a8984
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 1EP6R5562J
  • ID3Z1X61WY
  • 70FD1KFU70
  • 95IT3W8JZE
  • 118OYG6W3H
  • A4VZ22K1WT
  • 6IO182RP7A
  • F9S9FFU82N
  • S7V92P67HO
  • 56X6LID5ZY
  • 451W47IQ8X
  • I9I120531L
  • 398IYQ16YV
  • E0399OZS9N
  • SAA04E81UX
  • 7GL3G1COB3
  • AF73293C2R
  • U0NQ8555JD