NDC 69390-001

EAR RX

Aconitum Nap, Baryta Carb, Belladonna, Calc Carb, Capsicum, Carbo Veg, Causticum, Chamomilla, Ferrum Phos, Hepar Sulph Calc, Kali Mur, Lachesis, Lycopodium, Mercurius Sol, Natrum Mur, Plantago, Pulsatilla, Silicea, Sulphur, Verbascum

EAR RX is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Miami Beach Pediatrics Pa. The primary component is Aconitum Napellus; Barium Carbonate; Atropa Belladonna; Oyster Shell Calcium Carbonate, Crude; Capsicum; Activated Charcoal; Causticum; Matricaria Recutita; Ferrosoferric Phosphate; Calcium Sulfide; Potassium Chloride; Lachesis Muta Venom; Lycopodium Clavatum Spore; Mercurius Solubilis; Sodium Chloride; Plantago Major; Pulsatilla Vulgaris; Silicon Dioxide; Sulfur; Verbascum Thapsus.

• Product ID: 69390-001_167a8516-c207-4f62-93b2-edeeb9764bdd
• NDC: 69390-001
• Product Type: Human Otc Drug
• Proprietary Name: EAR RX
• Generic Name: Aconitum Nap, Baryta Carb, Belladonna, Calc Carb, Capsicum, Carbo Veg, Causticum, Chamomilla, Ferrum Phos, Hepar Sulph Calc, Kali Mur, Lachesis, Lycopodium, Mercurius Sol, Natrum Mur, Plantago, Pulsatilla, Silicea, Sulphur, Verbascum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-11-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Miami Beach Pediatrics pa
• Substance Name: ACONITUM NAPELLUS; BARIUM CARBONATE; ATROPA BELLADONNA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CAPSICUM; ACTIVATED CHARCOAL; CAUSTICUM; MATRICARIA RECUTITA; FERROSOFERRIC PHOSPHATE; CALCIUM SULFIDE; POTASSIUM CHLORIDE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; SODIUM CHLORIDE; PLANTAGO MAJOR; PULSATILLA VULGARIS; SILICON DIOXIDE; SULFUR; VERBASCUM THAPSUS
• 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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69390-001-01

30 mL in 1 BOTTLE, DROPPER (69390-001-01)

• Marketing Start Date: 2017-11-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69390-001-01 [69390000101]

EAR RX LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-11-22

Drug Details

Active Ingredients

Ingredient	Strength
ACONITUM NAPELLUS	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: a8753f88-4b8a-472f-a4bd-f2e9cec83610
• Manufacturer:
  • Miami Beach Pediatrics pa
• UNII:
  • 6P669D8HQ8
  • DD5FO1WKFU
  • ETJ7Z6XBU4
  • I76KB35JEV
  • C88X29Y479
  • C9TD27U172
  • 70FD1KFU70
  • 324Y4038G2
  • 91GQH8I5F7
  • WQZ3G9PF0H
  • 660YQ98I10
  • VSW71SS07I
  • 451W47IQ8X
  • 00UK7646FG
  • 2E32821G6I
  • W2469WNO6U
  • G0R4UBI2ZZ
  • 1MBW07J51Q
  • 2P3VWU3H10
  • U0NQ8555JD