NDC 58066-7022

Diarrhea Response

Aloe Socotrina, Chamomilla, Cinchona Officinalis, Colocynthis, Colostrum, Croton Tiglium, Cuprum Arsenicosum, Gelsemium Sempervirens, Ipecacuanha, Nux Vomica, Phosphoricum Acidum, Podophyllum Peltatum, Veratrum Album

Diarrhea Response is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Beaumont Bio Med. The primary component is Aloe; Matricaria Recutita; Cinchona Officinalis Bark; Citrullus Colocynthis Fruit Pulp; Bos Taurus Colostrum; Croton Tiglium Seed; Cupric Arsenite; Gelsemium Sempervirens Root; Ipecac; Strychnos Nux-vomica Seed; Phosphoric Acid; Podophyllum; Veratrum Album Root.

• Product ID: 58066-7022_0ddfb6a6-e5f0-472a-a4a1-789fbb71ea36
• NDC: 58066-7022
• Product Type: Human Otc Drug
• Proprietary Name: Diarrhea Response
• Generic Name: Aloe Socotrina, Chamomilla, Cinchona Officinalis, Colocynthis, Colostrum, Croton Tiglium, Cuprum Arsenicosum, Gelsemium Sempervirens, Ipecacuanha, Nux Vomica, Phosphoricum Acidum, Podophyllum Peltatum, Veratrum Album
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2011-09-08
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Beaumont Bio Med
• Substance Name: ALOE; MATRICARIA RECUTITA; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; BOS TAURUS COLOSTRUM; CROTON TIGLIUM SEED; CUPRIC ARSENITE; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PODOPHYLLUM; VERATRUM ALBUM ROOT
• 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 58066-7022-7

59.2 mL in 1 BOTTLE, SPRAY (58066-7022-7)

• Marketing Start Date: 2011-09-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58066-7022-7 [58066702207]

Diarrhea Response LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-09-08
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALOE	10 [hp_X]/59.2mL

OpenFDA Data

• SPL SET ID: e1fb4ac9-801d-4cb1-acec-01da476ca7bc
• Manufacturer:
  • Beaumont Bio Med
• UNII:
  • 23H32AOH17
  • S003A158SB
  • V5VD430YW9
  • SK8L60BCSQ
  • 2S713A4VP3
  • 0HK2GZK66E
  • E4GA8884NN
  • 639KR60Q1Q
  • QNS6W5US1Z
  • 62I3C8233L
  • G0R4UBI2ZZ
  • S256WJ3OFQ
  • 269XH13919