NDC 63736-324

Auro Earache Relief

Matricaria Recutita, Plantago Major, Verbascum Thapsus, Atropa Belladonna, Chili Pepper, Oyster Shell Calcium Carbonate, Crude, And Potassium Dichromate

Auro Earache Relief is a Auricular (otic) Liquid in the Human Otc Drug category. It is labeled and distributed by Insight Pharmaceuticals. The primary component is Matricaria Recutita; Plantago Major; Verbascum Thapsus; Atropa Belladonna; Chili Pepper; Oyster Shell Calcium Carbonate, Crude; Potassium Dichromate.

Product ID63736-324_67d0e4a6-91ac-4aac-bc2d-87cbc131529a
NDC63736-324
Product TypeHuman Otc Drug
Proprietary NameAuro Earache Relief
Generic NameMatricaria Recutita, Plantago Major, Verbascum Thapsus, Atropa Belladonna, Chili Pepper, Oyster Shell Calcium Carbonate, Crude, And Potassium Dichromate
Dosage FormLiquid
Route of AdministrationAURICULAR (OTIC)
Marketing Start Date2010-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameInsight Pharmaceuticals
Substance NameMATRICARIA RECUTITA; PLANTAGO MAJOR; VERBASCUM THAPSUS; ATROPA BELLADONNA; CHILI PEPPER; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM DICHROMATE
Active Ingredient Strength4 mL/30mL; mL/30mL; mL/30mL; mL/30mL; mL/30mL; mL/30mL; mL/30mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63736-324-24

24 BOX in 1 CASE (63736-324-24) > 1 BOTTLE in 1 BOX > 30 mL in 1 BOTTLE
Marketing Start Date2010-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63736-324-24 [63736032424]

Auro Earache Relief LIQUID
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-06-01
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
MATRICARIA RECUTITA4 mL/30mL

OpenFDA Data

SPL SET ID:e5a21e5c-75c8-4ccd-8a3d-919ea0078063
Manufacturer
UNII
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.