NDC 58066-7014

Sore Throat and Laryngitis Response

Aconitum Napellus, Antimonium Crudum, Arum Triphyllum, Borax, Causticum, Ferrum Phosphoricum, Graphites, Hepar Sulphuris Calcareum, Kali Bichromicum, Lac Defloratum, Phosphorus, Selenium Metallicum, Spongia Tosta

Sore Throat and Laryngitis Response is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Beaumont Bio Med. The primary component is Aconitum Napellus; Antimony Trisulfide; Arisaema Triphyllum Root; Sodium Borate; Causticum; Ferrosoferric Phosphate; Graphite; Calcium Sulfide; Potassium Dichromate; Skim Milk; Phosphorus; Selenium; Spongia Officinalis Skeleton, Roasted.

• Product ID: 58066-7014_dc668798-dd9b-4af5-be07-3877c8462cc4
• NDC: 58066-7014
• Product Type: Human Otc Drug
• Proprietary Name: Sore Throat and Laryngitis Response
• Generic Name: Aconitum Napellus, Antimonium Crudum, Arum Triphyllum, Borax, Causticum, Ferrum Phosphoricum, Graphites, Hepar Sulphuris Calcareum, Kali Bichromicum, Lac Defloratum, Phosphorus, Selenium Metallicum, Spongia Tosta
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2011-12-20
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Beaumont Bio Med
• Substance Name: ACONITUM NAPELLUS; ANTIMONY TRISULFIDE; ARISAEMA TRIPHYLLUM ROOT; SODIUM BORATE; CAUSTICUM; FERROSOFERRIC PHOSPHATE; GRAPHITE; CALCIUM SULFIDE; POTASSIUM DICHROMATE; SKIM MILK; PHOSPHORUS; SELENIUM; SPONGIA OFFICINALIS SKELETON, ROASTED
• Active Ingredient Strength: 10 [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58066-7014-7

59.2 mL in 1 BOTTLE, SPRAY (58066-7014-7)

• Marketing Start Date: 2011-12-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58066-7014-7 [58066701407]

Sore Throat and Laryngitis Response LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-20
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ACONITUM NAPELLUS	10 [hp_X]/59.2mL

OpenFDA Data

• SPL SET ID: 638a0838-ccd8-4e7d-a2ed-144506185bbe
• Manufacturer:
  • Beaumont Bio Med
• UNII:
  • DD5FO1WKFU
  • 6A001Y4M5A
  • DM64K844DM
  • 91MBZ8H3QO
  • 91GQH8I5F7
  • H6241UJ22B
  • 4QQN74LH4O
  • T4423S18FM
  • F79059A38U
  • 27YLU75U4W
  • 1MBW07J51Q
  • 1PIP394IID
  • U0NQ8555JD