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 ID69390-001_167a8516-c207-4f62-93b2-edeeb9764bdd
NDC69390-001
Product TypeHuman Otc Drug
Proprietary NameEAR RX
Generic NameAconitum 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 FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-11-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameMiami Beach Pediatrics pa
Substance NameACONITUM 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 Strength6 [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 FlagN
Listing Certified Through2020-12-31

Packaging

NDC 69390-001-01

30 mL in 1 BOTTLE, DROPPER (69390-001-01)
Marketing Start Date2017-11-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69390-001-01 [69390000101]

EAR RX LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-22

Drug Details


Trademark Results [EAR RX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EAR RX
EAR RX
78446643 2956331 Dead/Cancelled
Le, Bruce
2004-07-06

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