NDC 15631-0067

AURUM MURIATICUM NATRONATUM

Aurum Muriaticum Natronatum

AURUM MURIATICUM NATRONATUM 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 Sodium Tetrachloroaurate.

Product ID15631-0067_5e446de1-fe9a-48b9-a5ad-d731229577ce
NDC15631-0067
Product TypeHuman Otc Drug
Proprietary NameAURUM MURIATICUM NATRONATUM
Generic NameAurum Muriaticum Natronatum
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 NameSODIUM TETRACHLOROAURATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0067-0

100 PELLET in 1 PACKAGE (15631-0067-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0067-5 [15631006705]

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

NDC 15631-0067-0 [15631006700]

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

NDC 15631-0067-1 [15631006701]

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

NDC 15631-0067-4 [15631006704]

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

NDC 15631-0067-2 [15631006702]

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

NDC 15631-0067-3 [15631006703]

AURUM MURIATICUM NATRONATUM 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
SODIUM TETRACHLOROAURATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:1a8104dc-61c7-4238-8dfe-5b8350c44ffa
Manufacturer
UNII

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

NDCBrand NameGeneric Name
0220-0648Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
0220-0649Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
0220-0650Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
15631-0067AURUM MURIATICUM NATRONATUMAURUM MURIATICUM NATRONATUM
15631-0529AURUM MURIATICUM NATRONATUMAURUM MURIATICUM NATRONATUM
63545-317Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-318Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-319Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-320Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-321Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-322Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-323Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-324Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-325Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
63545-653Aurum muriaticum natronatumAurum muriaticum natronatum
68428-242Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
71919-103Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE

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