NDC 15631-0066

AURUM MURIATICUM

Aurum Muriaticum

AURUM MURIATICUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Gold Trichloride.

Product ID15631-0066_908de8b0-f3f8-4983-b7d7-0412abe0a49f
NDC15631-0066
Product TypeHuman Otc Drug
Proprietary NameAURUM MURIATICUM
Generic NameAurum Muriaticum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGOLD TRICHLORIDE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0066-0

100 PELLET in 1 PACKAGE (15631-0066-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0066-3 [15631006603]

AURUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0066-0 [15631006600]

AURUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0066-1 [15631006601]

AURUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0066-4 [15631006604]

AURUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0066-5 [15631006605]

AURUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0066-2 [15631006602]

AURUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

Drug Details

Active Ingredients

IngredientStrength
GOLD TRICHLORIDE3 [hp_X]/1

OpenFDA Data

SPL SET ID:22fe7766-64d8-4973-adc0-cfd6bf50a5af
Manufacturer
UNII

NDC Crossover Matching brand name "AURUM MURIATICUM" or generic name "Aurum Muriaticum"

NDCBrand NameGeneric Name
0220-0640Aurum muriaticumGOLD TRICHLORIDE
0220-0674Aurum muriaticumGOLD TRICHLORIDE
0220-0675Aurum muriaticumGOLD TRICHLORIDE
0220-0676Aurum muriaticumGOLD TRICHLORIDE
0220-0677Aurum muriaticumGOLD TRICHLORIDE
15631-0066AURUM MURIATICUMAURUM MURIATICUM
63545-308Aurum MuriaticumAurum Muriaticum
63545-309Aurum MuriaticumAurum Muriaticum
63545-310Aurum MuriaticumAurum Muriaticum
63545-311Aurum MuriaticumAurum Muriaticum
63545-312Aurum MuriaticumAurum Muriaticum
63545-313Aurum MuriaticumAurum Muriaticum
63545-314Aurum MuriaticumAurum Muriaticum
63545-315Aurum MuriaticumAurum Muriaticum
63545-316Aurum MuriaticumAurum Muriaticum
68428-241Aurum muriaticumGOLD TRICHLORIDE
71919-102Aurum muriaticumGOLD TRICHLORIDE

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